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Shorty
Thank you for your take on this.
Shorts, are you trying to cover, I think so. You keep waiting it'll cost you more to cover, at your own peril. imo.
Someone is loading up on these cheap shares. Just a matter of time before things heat up. imo.
Bought back in, lets go!
I added to my position, couldn't pass up on these prices, long and strong.
5. Conclusion of Law 37 of D.15-09-004 does not fully reflect the text on page 29 of D.15-09-004. Conclusions of Law 1. The proposed modifications to Decision 15-09-004 are consistent with D.14-10-081. 2. D.15-09-004 and the standard contract should be modified to affirm that directed biogas is eligible for BioMAT, provided that the proposed projects meet all other program requirements. 3. Directed biogas in the BioMAT Program may include any fuel source identified in Pub. Util. Code § 399.20(f)(2) that is also an eligible feedstock pursuant to CEC’s RPS eligibility rules. 4. FCE and Toyota’s Petition for Modification of D.15-09-004 should be granted. O RDER IT IS ORDERED that: 1. The Petition for Modification of Decision 15-09-004 is granted. 2. Decision 15-09-004 is modified as follows: a. Conclusion of Law 37 in D.15-09-004 is revised to read as follows:
R.15-02-020 ALJ/NIL/ML2/gp2 PROPOSED DECISION (Rev. 1)
- 16 -
Because it is consistent with the requirements of D.13-11-024, section 3.1.1 of the BioMAT standard contract submitted on February 9, 2015 should be approved as submitted on February 9, 2015 and included in the final BioMAT standard Contract, renumbered to be section 3.1 (and as it may be subsequently renumbered). It will apply to all eligible BioMAT projects using biomethane delivered through a common carrier pipeline.
b. Conclusion of Law 53 is added to D.15-09-04 and reads as follows: BioMAT projects using biomethane delivered through a common carrier pipeline should be eligible for a BioMAT PPA, provided they meet all applicable BioMAT program requirements. 3. Not later than 45 days from the date of this decision, Southern California Edison Company, San Diego Gas & Electric Company, and Pacific Gas and Electric Company are directed to each file a Tier 2 Advice Letter modifying its corresponding BioMAT Power Purchase Agreement to conform with today’s decision that clarifies directed biogas is eligible under BioMAT by incorporating the new language specified in Section 4.2.3 and incorporating reporting requirements that are consistent with the California Energy Commission’s Renewables Portfolio Standard Eligibility Guidebook. 4. Rulemaking 15-02-020 remains open to resolve outstanding issues. This order is effective today. Dated , at San Francis
DECN starting to have life
FCEL, I think bottomed, going back up.
FCEL,I sure am holding, this is a hold, I'm in long term. Have a great day.
fcel Moving up!!
DECN coming off its low?
RTTR Chart
RTTR On the move, big vol.
FCEL going crazy!!! Go FCEL
Yes it has!
FCEL Looks like it will hit a dollar or more today!
FCEL could become another Apple or Amazon or one of those super big companies. It's in a growing field.
I'm with you, skies the limit on this one.
FCEL Moving up
I like what I'm hearing.
Shorts will have to cover sooner or later. They have to much going for them. imo.
Be patient and longs will be rewarded. imo.
The company has good products, it's FDA approved and has the CE mark. Need to give it time and this will go much much higher.I wouldn't dare to be short on this. imo.
Looks like it might of bottomed, looking good.
On Fox news today, I saw a Soldier that was injured. They showed him in a exoskeleton and they said he can walk now. Is the VA paying for the exoskeleton now for service members?
They do need to do something about short selling. It's to easy for these Hedge funds to kill a stock.
Poster from other board.
betasplen2 hours ago
The whole float has already traded in less than 30 min! This is wonderful news that Cigna has started approving the use for civilians. The $18M backlog can now start clearing quickly and with the expected Restore approval worldwide in a few months, they will go head to head with EKSO and hopefully get a similar valuation ($15/share) by 3Q or as well.
Looks like a go from here!
From other board...
betasplen2 hours ago
The Exo Restore for stroke victims will be launching in Europe in a couple of months (pending CE approval which should be almost a given) and in early 3Q if the FDA approves for use in the US. They have several units awaiting insurance approval and with the recent change in Cigna's policy, they should be winning a good % of them. Same with the VA as the training has been completed for the veterans. They have reduced cash burn significantly in 2018 and said they will do even better this year. With the cash in hand, they can hit the ground running with order fulfillment. The Restore is only $12K (vs $100K for the current device). The market is huge with 750K stroke victims in the US alone. Do the math - that is $9B in market potential! I think they can conservatively do $25M in sales this year. Currently, they are trading at only a $18M market cap. I think this can get to $15 by Christmas ($72M) and easily over $50 ($200M) next year if Restore sells as expected...
DECN Hails Completion of Its Genultimate! TBG Panacea System, 3rd Party Testing to Begin in Next 7 Days, Clinical Trials Testing to Begin in May
ACCESSWIRE•April 4, 2019
Equity Fund in Stealthy Move Tried to Gain Control of DECN In March, Just as a Big Box Was in Contact to Buy Genultimate TBG When Available, Sight Unseen
LOS ANGELES, CA / ACCESSWIRE / April 4, 2019 / Decision Diagnostics Corp. (OTC PINK: DECN) Decision Diagnostics Corp. is a 17 year old diabetes focused bio-technology R&D firm, manufacturer, quality plan administrator, FDA registered medical device customer support organization, and exclusive worldwide sales and regulatory process agent for a growing brand of glucose test strips and meters as highly accurate alternatives for legacy diabetic, proprietary, and pet testing glucose test strips.
Decision Diagnostics is pleased to announce and communicate that the company's GenUltimate! TBG test strip and meter, the next generation panacea at-home testing product for diabetics, has completed its advanced development and begun testing for verification in advance of third party testing and patient clinical trials as a part of the company's application for 510K clearance through the U.S. FDA.
Keith Berman, CEO of DECN commented, "The completion of GenUltimate! TBG is the seminal product development event in the company's history. This product is the answer to our plans and marks a watershed event in an industry awash with older technology and ‘me-too' products, typically designed in haste, for the singular purpose of gaining access to the huge and growing U.S. at home diabetic testing market. We view GenUltimate! TBG as a product where the market has reversed the value proposition and elected instead to gain access to our panacea product under the pretext of "those guys were able to do it and by-god it works.""
GenUltimate! TBG technology is designed to correct for Hematocrit (HCT) interference inherent in all at-home testing methodologies. By accomplishing this correction, GenUltimate! TBG offers precision and accuracy wished for, but virtually unheard of in at-home testing of diabetics. In fact, in several of our recent verification testing, GenUltimate! TBG out-performed even the reference methodology. This is quite the accomplishment.
Setting its own standard, GenUltimate! TBG will be capable of reporting glucose results at a reproducible rate of +/- 8.0%, in an industry where +/- 15% is not only the norm but also the published FDA guidance specifications. The company plans patent applications as soon as a current round of financing is accomplished. The GenUltimate! TBG technology will also be used as an enhancement to our GenUltimate! and GenUltimate! 4Pets test strips, now in worldwide commercial use.
Mr. Berman continued, "As stated previously we are putting all available resources and energy into our quickly growing product lines. We now recognize the value in use of our GenUltimate! TBG product and technology. To one company that has already contacted us, GenUltimate! TBG can be viewed as up to a $1.5 billion value add to a particular market leader. And while we have had discussions with a well branded big box, as GenUltimate! TBG grows closer to commercial availability, we expect contact with all of the major big box companies, that is if we choose not to license our panacea product to an august market leader."
The company's current portfolio of test strips includes its market established GenUltimate!, plus its GenChoice!, GenSure!, and GenUltimate! TBG test strips, its Avantage! and Precise! Glucometers, and its PetSure! and GenUltimate! 4Pets testing products for dogs, cats and horses. The company's GenChoice! test strips are part of a current 510K prosecution process with the U.S. FDA.
ABOUT DECISION DIAGNOSTICS CORP
Decision Diagnostics Corp. is the leading manufacturer and worldwide distributor of diabetic test strips engineered to operate on legacy glucose meters. DECN's products are designed to operate efficiently and less expensively on certain glucose meters already in use by almost 7.5 million diabetics worldwide. With new inspired technology diabetic test strips already in the final stages of development, DECN products compete on a worldwide scale with legacy manufacturers currently selling to 71+ percent of a $12 billion at-home testing market.
Forward-Looking Statements
This release contains the company's forward-looking statements which are based
NEW YORK, NY / ACCESSWIRE / April 1, 2019 / Traders News Source, a leading independent equity research and corporate access firm focused on small and mid-cap public companies is issuing a comprehensive report on ReWalk Robotics, Ltd. (RWLK), a company that develops, manufactures and markets wearable robotic exoskeletons for individuals with lower limb disabilities as a result of spinal cord injury (SCI) or stroke.
There have been 500 systems placed, with the majority for home and community use; other systems used in rehab centers.
There is a substantial market for the company's ReWalk exoskeleton for SCI patients in the U.S. with a substantial backlog of demand.
Will your insurance cover an exoskeleton if you are paralyzed by a SCI?READ MORE
Copy and paste to your browser may be required to view the report - https://tradersnewssource.com/rewalk-robotics-2/
On March 26, 2019, the company announced the delivery of a ReWalk Personal 6.0 System to Lucy Dodd, a British children's social care worker paralyzed by a rare spinal condition, which will allow her to stand and walk again. The ReWalk exoskeleton - a medical device designed for individuals with spinal cord injury to be used in the home and the community - is in use throughout the UK and around the world. Lucy Dodd will begin rehabilitation training after national fundraising campaign with support from the Association for the Independence of Disabled People.
Read about near term developments at RWLK and get the analysts target price READ MORE
Copy and paste to your browser may be required to view the report - https://tradersnewssource.com/rewalk-robotics-2/
This document is not intended as an offering, recommendation, or a solicitation of an offer to buy or sell the securities mentioned or discussed and is to be used for informational purposes only. Please read all associated disclosures and disclaimers in full before investing. Neither TNS nor any party affiliated with us is a registered investment adviser or broker-dealer with any agency or in any jurisdiction whatsoever. To download our report(s), read our disclosures, or for more information, visit https://www.tradersnewssource.com.
CFA® and Chartered Financial Analyst® are registered trademarks owned by CFA Institute.
CONTACT: editor@tradersnewssource.com
SOURCE: Traders News Source
View source version on accesswire.com:
https://www.accesswire.com/540702/Will-Your-Insurance-Pay-for-a-ReWalk-Robotics-Solution-for-Paralysis
British Paraplegic Receives ReWalk Exoskeleton Device After Successful Campaign to Walk Again
PR Newswire•March 26, 2019
Lucy Dodd will begin rehabilitation training after national fundraising campaign with support from the Association for the Independence of Disabled People
BIRMINGHAM, England and YOKNEAM ILIT, Israel, March 26, 2019 /PRNewswire/ -- ReWalk Robotics, Ltd. (RWLK) ("ReWalk" or the "Company"), a leading manufacturer of robotic medical devices for individuals with lower limb disabilities, today announced delivery of a ReWalk Personal 6.0 System to Lucy Dodd, a British children's social care worker paralyzed by a rare spinal condition, which will allow her to stand and walk again. The ReWalk exoskeleton—a medical device designed for individuals with spinal cord injury to be used in the home and the community—is in use throughout the UK and around the world.
The system is being delivered following a successful fundraising campaign, led by Dodd and supported by the Association for the Independence of Disabled People (AID), a small Cumbrian charity which aims to improve accessibility in society for the disabled. The Lucy's Legs campaign brought in a range of donors, and ran varied activities culminating in a sponsored abseil at Spinnaker Tower in Portsmouth on 23rd March. Dodd, who works as a child services officer for Hampshire County Council, suffered a rare spinal condition, Arteriovenous Malformation, when she was 18. After a series of operations, she lost the use of her legs, and has been confined to a wheelchair for 14 years. Doctors told her she would never walk again.
"This is a major step in a years' long battle to change the definition of possible,'' said Dodd. 'Standing tall and walking again with ReWalk will be a lease of freedom every day and I am incredibly excited to start this new chapter. I would like to thank everyone who put time, effort and of course funds into this battle, including and especially the tireless Ruth and Paul Adorian from AID''.
Dodd was introduced to ReWalk's revolutionary technology in 2017 and began campaigning in 2018, with AID serving as the largest donor to Lucy's Legs.
Paul Adorian, Managing Director of AID said, "Our mission is to empower disabled people and today certainly feels like a milestone. AID is built in the image of our Founder, the Hon. Mrs. Ruth Adorian, who was diagnosed with Motor Neurone Disease but has used her experience to help others. Lucy's ReWalk exoskeleton will create a miracle by providing almost natural mobility to someone who thought that their life could never be the same again. We are delighted to work with ReWalk and look forward to helping many more people regain mobility and freedom.''
Upon receipt of the system, Lucy will begin the standard training modules at Hobbs Rehabilitation Centre in Winchester to learn to use her system at home and in her daily life activities. ReWalk will support Dodd through the required training for home and community use of the system.
More than 50,000 people in the UK and Ireland are seriously disabled due to spinal damage following an accident, and the great majority now face the prospect of being confined to a wheelchair for the rest of their lives.
"Lucy's campaign to walk again has been inspirational and is testament first and foremost to her determination and resilience," said Larry Jasinski, CEO of ReWalk Robotics. "ReWalk is delighted to have the opportunity to work with AID in supporting Lucy and others to access life-changing exoskeleton technology. We are always proud to welcome exceptional ReWalkers into our growing family."
ReWalk Robotics Personal 6.0 is a wearable robotic exoskeleton that provides powered hip and knee motion to enable individuals with spinal cord injury to stand upright and walk. ReWalk is the first exoskeleton system to receive FDA clearance for use in the home as well as in the rehabilitation setting. ReWalk received a CE mark in June 2010, and FDA clearance in June 2014.
About ReWalk Robotics Ltd.
ReWalk Robotics Ltd. develops, manufactures and markets wearable robotic exoskeletons for individuals with spinal cord injury. Our mission is to fundamentally change the quality of life for individuals with lower limb disability through the creation and development of market leading robotic technologies. Founded in 2001, ReWalk has headquarters in the U.S., Israel and Germany. For more information on the ReWalk systems, please visit www.rewalk.com.
Continue reading
ReWalk® is a registered trademark of ReWalk Robotics Ltd. in Israel.
About AID
AID, the Association for the Independence of Disabled People, is a charity that aims to improve the lives of people living with a disability. Founded by The Hon. Mrs Ruth Adorian, who was diagnosed with Motor Neurone Disease (MND) in 2007, the charity aims to change the little things that make a big difference to people with disabilities. AID objectives include improving facilities for disabled people and supporting research into new drugs for diseases which are currently looked upon as incurable.
Currently AID is involved in the provision of the ReWalk exoskeleton to people who have been deprived of the ability to walk following accident or illness, but also in an exciting new project where dogs will be trained to diagnose MND in humans, in the hope that before too long, a drug will be identified which will prove to benefit MND sufferers making it all the more important that the diagnosis time of this horrible disease can be drastically reduced.
These projects rely primarily on the generosity of donations from trusts and the public and the possibilities for helping more people with problems such as these are limited almost entirely by funding.
For press enquiries or interviews contact Mr Paul Adorian, Managing Director on 01539448459 or email: paul@dday.org.uk
For more information visit: www.disabledday.org or write to:
AID
Applethwaite Lodge
Windermere
Cumbria
LA23 1JQ
For membership forms and donations contact Mr Paul Adorian at the above address, telephone number or email
Association for the Independence of Disabled People (AID) is a Charitable Company Limited By Guarantee. Charity Commission Registration number: 1158537
Founder and Chairman, Mrs Ruth Adorian. AID founded, 28 May 2014
Forward-Looking Statements
In addition to historical information, this press release contains forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, Section 27A of the U.S. Securities Act of 1933, and Section 21E of the U.S. Securities Exchange Act of 1934. Such forward-looking statements may include projections regarding ReWalk's future performance and, in some cases, may be identified by words like "anticipate," "assume," "believe," "continue," "could," "estimate," "expect," "intend," "may," "plan," "potential," "predict," "project," "future," "will," "should," "would," "seek" and similar terms or phrases. The forward-looking statements contained in this press release are based on management's current expectations, which are subject to uncertainty, risks and changes in circumstances that are difficult to predict and many of which are outside of ReWalk's control. Important factors that could cause ReWalk's actual results to differ materially from those indicated in the forward-looking statements include, among others: ReWalk's ability to secure capital from its equity and debt financings in light of limitations under its Form S-3, the price range of its ordinary shares and conditions in the financial markets, and the risk that such financings may dilute ReWalk's shareholders or restrict its business; ReWalk's ability to regain compliance with the continued listing requirements of the Nasdaq Capital Market and the risk that its ordinary shares will be delisted if it cannot do so; ReWalk's expectations regarding future growth, including its ability to increase sales in its existing geographic markets, and to expand to new markets and achieve its planned expense reductions; the conclusion of ReWalk's management and the opinion of ReWalk's auditors in that there are substantial doubts as to ReWalk's ability to continue as a going concern; ReWalk's ability to maintain and grow its reputation and the market acceptance of its products; ReWalk's ability to achieve reimbursement from third-party payors for its products; ReWalk's limited operating history and its ability to leverage our sales, marketing and training infrastructure; ReWalk's expectations as to its clinical research program and clinical results; ReWalk's ability to improve its products and develop new products; ReWalk's ability to repay its secured indebtedness; the outcome of ongoing shareholder class action litigation relating to ReWalk's initial public offering; ReWalk's compliance with medical device reporting regulations to report adverse events involving its products and the potential impact of such adverse events on ReWalk's ability to market and sell its products; ReWalk's ability to gain and maintain regulatory approvals; ReWalk's expectations as to the results of, and the Food and Drug Administration's potential regulatory developments with respect to, ReWalk's mandatory post-market 522 surveillance study and ReWalk's 510k submission for the ReStore for stroke patients; ReWalk's ability to maintain adequate protection of its intellectual property and to avoid violation of the intellectual property rights of others; the risk of a cybersecurity attack or breach of our IT systems significantly disrupting our business operations; the risk that the remaining Timwell Corporation Limited ("Timwell") issuances will fail to close and the China joint venture will not form, and the resulting effect on ReWalk's liquidity and financial condition; the risk of substantial dilution resulting from additional issuances, if any, to Timwell; the significant voting power and de facto voting control Timwell may acquire upon additional issuances, if any; ReWalk's ability to use effectively the proceeds of offerings of securities; ReWalk's ability to maintain relationships with existing customers and develop relationships with new customers; the impact of the market price of ReWalk's ordinary shares on the determination of whether ReWalk is a passive foreign investment company; and other factors discussed under the heading "Risk Factors" in ReWalk's Annual Report on Form 10-K for the fiscal year ended December 31, 2018 filed with the U.S. Securities and Exchange Commission (the "SEC") and other documents subsequently filed with or furnished to the SEC. Any forward-looking statement made in this press release speaks only as of the date hereof. Factors or events that could cause ReWalk's actual results to differ from the statements contained herein may emerge from time to time, and it is not possible for ReWalk to predict all of them. Except as required by law, ReWalk undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future developments or otherwise.
From other board...
Stephen4 hours ago
Thank you for reaching out.
As we navigate our way through this everchanging Blockchain technology sector management will be concentrating our focus on certain aspects as we move forward. We hope to provide investors with an update soon.
Here are a few initiatives we have on the go:
We have recently closed on 60% ownership for SV CryptoLab which is currently mining.
Invested $1 Million into Arcology, which is putting together a team of programmers to develop our own Blockchain
LOI to develop Pressland into a blockchain powered fake news fighter for the media industry
Initiated a partnership with Epic Blockchain, a company developing new processors for optimal hashrates.
Initiated a partnership with NOS Blockchain, a subsidiary of Nerds on Site, a tech support company.
You can read our latest press releases by clicking the link below:
http://www.360blockchaininc.com/news
I will also add your email to our company email database and keep you informed with company news and will send you our Investors presentation as soon as its completed.
I hope that this helps and feel free to call or email if you require any additional details.
Thank you,
Anil Mall
I also think it's time to load. imo.
I agree with you
The article then is confusing.