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Did Dean forget to put you on the list for the memo? I've been telling you for months to buy in before the runup begins. Its not too late. Get IMGG while it is still relatively cheap.
I agree lobcrab, while there are a few daytraders out there doing the wash, rinse, repeat cycle, others are just getting back in before the runup starts (whick it already has).
Tell me when you go straight to the SEC about this.
What is the basis of your complaint? I'm sure either they have heard whatever you are complaining about before and its not a problem.
JANES' ARMY OF CONSULTANTS----
everyone is busy and doesn't want to be bothered by nonsense. Thats why they have not be named. You will know soon enough.
I agree, Its lookin real good for Dean! IMGG has the financing they need. BK will not happen. The meeting with the FDA and consultants is a huge step in the right direction. The next FDA filing will be the best chance yet at approval.
Owl, there is no proof of Dean selling 27M shares of IMGG because he didn't sell anything. If he did, the proof would have been posted by now and volume is less than 1M per day anyway, so how could he sell without anyone seeing it. I would not believe what is posted unless there is some kind of proof behind it.
I asked for proof and none was given. It is just suspicions and accusations. There is no proof Dean sold 27M shares of IMGG or even one share for that matter. I will not belive this to be the case until someone can post proof.
Wow, that is a serious accusation AT. What proof do you have about any of Dean's stock trading? I still haven't seen proof of your accusation of the 27.6M shares. Do you have some proof or is this just a speculation of yours?
still no proof JANES HAS SOLD 27.6M SHARES SINCE FDA LETTER. This was posted as if it was a fact but I don't see any proof!
please show us where JANES HAS SOLD 27.6M SHARES SINCE FDA LETTER
F.D.A. Plans to Streamline Reviews of Medical Devices
http://www.nytimes.com/2011/01/20/business/20device.html
............. The F.D.A. said it would impose 25 changes to the device-approval process, including streamlining the reviews for some lower-risk devices. The agency also will also create an internal council to “assure timely and consistent science-based decision making.”
The steps will lead to “a smarter medical device program that supports innovation, keeps jobs here at home, and brings important, safe and effective technologies to patients quickly,” said Dr. Jeffrey Shuren, head of the F.D.A. device unit.
the investment thesis behind buying a stock whose only product is dependent on FDA approval is based on the fact that the FDA is finally waking up to the fact that their own process sucks. This is the NEW FDA, so between the new FDA process and the consultants dotting the I's and crossing the T's, this has a good chance for approval this time around.
The FDA seems to be doing a terrible job of approving devices that actually work !!
http://articles.baltimoresun.com/2011-02-24/news/bs-ed-fda-regulations-20110224_1_diseased-heart-valves-cardiology-fda
A study conducted by John Makower, consulting associate professor at Stanford's Biodesign Innovation program, demonstrated that the FDA delays approval by two years, on average, for low-to-medium-risk medical devices, compared with Europe; approval of high-risk devices in the U.S. took 31/2 years longer than in Europe.
Perhaps in response, the FDA finally announced this month its openness to considering reforms to the review process for innovative medical devices. The current premarket review process for new medical devices has been fraught with uncertainty, often requiring companies to produce further unanticipated testing and data for proven products. Regulations force device manufacturers to replicate time- and cost-consuming studies in the U.S., despite the existence of reputable equivalent scientific data gathered overseas.
In contrast to the FDA, the European Medical Devices Directive allows privatized, notified bodies to test device safety to provide the stamp of European market approval.
Last week, the House Energy and Commerce Committee's Subcommittee on Health held a hearing on medical device regulations. In his testimony, Mark Deem of San Francisco Bay area medical device incubator The Foundry blamed the unpredictability of FDA regulatory delays for driving U.S. business to Europe.
"We develop our products here and then run the same large, multicenter randomized trials we would otherwise have conducted in the U.S. overseas," he said. "We are then staying [in Europe] to commercialize the products while we decide when and if to approach the FDA."
Much of the bureaucracy inherent in the FDA approval process has been driven by calls for increased patient safety. However, despite the speed of the privatized European device approval process, there have been no sacrifices in patient safety. A report by the Boston Consulting Group released earlier this year found that the medical device recall rate was similar in the U.S. and Europe.
You can't have it both ways.
On one hand you say they can't be too close because of the radiation
On the other hand, you say slight of hand.
With 70 people there, I douby he could Hudini his way out of giving a real demo. Listen to lobcrab. This is a first hand eyewitness account. You are just providing speculation.
checkered flags, long and strong!
Janes and the FDA will be on the same page after the meeting and the submission will be completed without incident. The FDA will go through the submission and tell Dean what a nice job he did this time and the approval will follow.
Then, one of two things will happen, The DViS will be bought out from Toshiba or Dean will outsource the production of the device and will make tons of money and revolutionize the medical imaging insustry.
Yes, the checkered flag is in sight!
Long and Strong until the final Gong!
Sorry Lamb, I meant to say $0.50. IMGG is a stock that I like now because the upside is so huge! Based on the OH showing the DViS live and the consultants being on board and Dean checking his ego at the door are all good signs. We will see after the meeting with the FDA, but your $0.50 should be up to $1 or $2 soon enough, so be patient.
You have it right, this is exactly how it will go:
Dean and his army of consultants are meeting face to face with the FDA (in a couple weeks) and they are going to tell the FDA what they are going to submit, and the FDA is going to say looks good to us Dean. Then Dean will gather up his images, submit the package, and we're all gonna be rich. Phil and I will be rich having invested some staggering amounts, and you will be happy with a new fishing pole.
JANES IS NOT DECEIVING SHAREHOLDERS
He has a working Real Time 3D imaging device that will pass through the FDA now that he is using the consultants to get everything right and following the processes. His EGO has been set aside and he realized he was making too many mistakes doing this himself. He is ont he right track now.
The checkered flag will be waving soon!
Long and strong until the final gong!
Dean thanks you for your $50, he had a nice business lunch. Now, he is working through the rest of the process. Does it take money to do this? Of course it does. But the funding is in place and Dean will have it wrapped up shortly. The FDA will be on board after the meeting in mid October and the rest will be gravy. Your $50 will be multiplied many times over soon, so hold the shares for a nice profit or sell them now and get rid of your stress, its your choice. If you hold, you will be singing the praises of Dean soon enough.
yes, Let a Judge decide.
You have Dean pegged as Guilty until proven innocent. In case you missed the memo, thats not the way it goes in a court of law in the United States.
Dean Janes, Innocent until proven guilty in a court of law!
may have already happened?? The trading has been so light, this has not happened. The shares are being held.
CP, You have been gone for a while, so I will fill you in.... Dean had an open house where he showed the DViS performing its real time 3D scanning. Everyone who went witnessed this. He has funding available to get him through the next round of FDA submissions and hopefully approvals. Deans Ego has been squashed and now he has consultants on board who are making sure everything is ready and in good order. They are meeting with the FDA in Mid-October. Things are back on track now and you may be surprised by the results. Stay tuned.
Listen to the conference call again, the meeting with the FDA is in the middle of October.
Yes, Lamb, the finish line is in sight. Once Dean works with the FDA and he and the consultants nail this down, its just a matter of time before they will be waving the checkered flag and popping the corks.
The people I talked to from GE have a high opinion of Dean and respect his work. They thought it was funny when I told them that he was being talked about in such a negative manner.
So, what is the dosage of the DViS versus a Dental X-Ray. I'm curious how much different they are. To put it into perspective, how much radiation is there in a MRI?
I guess Dean was taking one for the team. How else can you get an x-ray than to go into the device. How about when someone gets an MRI and gets bombarded with huge doses of radiation. Remember, this is a low radiation device. Dean will not be glowing int he dark. Its probably about the same as getting a dental x-ray.
You could assume, but since the OH attendies signed a NDA, you could not be sure. Besides, apparently there was a distance requirement that was observed and I'm sure this was all checked out in advance. You could send a note to info@imaging3.com if you want more details about the open house. I would not presume anything at this point if I was not there.
Yes, it was real time 3D imaging
Yes, the DViS is real
Yes, the radiation from the DViS is low
Yes, the DViS is portable
Yes, the checkered flag will be waving soon for Dean, Imaging3 and the DViS!
If you didn't go, you don't know.
Long and Strong until the final gong!
Lamb, Phil told me he only has one post per day, but he and I have a load of shares in IMGG now and he will be buying more (I have maxed out). He and I discuss IMGG offline and we are both confident in the DViS and the pending FDA approval. We are pleased with the comments of those that attended the open house. If I had doubts, I would have gotten out a long time ago. If you have doubts, I recommend selling all your shares of IMGG and looking into a stock you have more confidence in.
GDS, where did you hear that Dean paid for the private jet? I still haven't seen proof that came out of of IMGG or Dean's pocket. Please show the proof.
I keep hearing talk about fraud at the open house, but those people did not attend the open house and have no idea what happened there, so its just talk. On the other hand, the people that went to the open house and saw the demo are saying it is not fraud. Which response should we believe? I think those who went to the open house have more credibility.
Dean may get fined if he didn't have the proper approvals. It is more likely everything was cleared with the proper officials and no laws were broken.
Dean will not likely get fined and he will certainly not be going to jail. It seems that all this is simply speculation and has been blown way out of proportion.
The DViS is real.
The DViS is a working real time 3D device.
The DViS is emits low radiation.
The DViS was demonstrated following all laws.
If you didn't go, you don't know.
The checkered flag will be waving for the DViS soon.
Lamb, According to FormerMarine who went to the open house, the technician had a radiation badge on that he showed to those standing near by. He can clarify in a reply as long as he stays on topic, but it seems the DViS generates some low dose radiation, but since Dean is permitted to run devices that emit radiation, he is permitted to do so as long as he stays within the guidelines and spectators were not exposed to the radiation. I'm sure that all the laws were followed and Dean will not be going to jail for this.
If you didn't go, you don't know.
The checkered flag is just over the horizon.
Please keep us posted on your report on IMGG to the California Department of Public Health. We're also still awiting to hear a post on the status of the SEC from another frequent poster here. We were told they would be knocking on Dean's door with a pair of handcuffs with his name on them. That has been in the works for over a year now and there is no update. The authorities must be real busy handling all the claims against Dean.
MEMO TO DEAN JANES: Your device is safe and effective!!! What's that???? You say that you have tested the Dvis and proved it works as you claim it does, so you decided to show a great demo and have consultants helping you submitting the correct paperwork to the FDA. The actions of a true scientist.
I guess that goes to show you, if you don't believe in the DViS all it takes is a visit to an open house and you will be a believer and a supporter after seeing a live demo of this break through real time 3d imaging device.
If you didn't go, you don't know.
The checkerd flag will wave for IMGG soon.
imrichbeotch, just tell us this much.
Was the real time 3D demo done legally or is Dean going to jail?
Do you trust Dean and are you happy with what you saw?
Do you see a checkered flag in Dean's future?
So, was the DViS behind a shield or far enough away so there was no radiation passed to the audience? Was the radiation monitored? Tell us how the OH was setup.
The buyers are all in now plus dean has financing. They do not need to sell the .05 PPM and they will not go to a .025 PPM. The price will go up from here making the .05 more attractive as FDA approval gets closer. Bankruptcy and extinction are not Imminent.
no need to sell .05 PPM's. Dean has the financing to get through the FDA approval. The checkered flag will wave soon.
I don't see over 99.9% of invesoters are UNDERWATER. I hear some people are under water, others bought in at .03 and are still good, some day trade and are doing well, some sold high and kept some and are still in the black. I don't think your estimate is even close.
WHAT PROOF DO YOU HAVE that the "SEC WILL CHARGE AND ARREST JANES SIMULTANEOUSLY"? I have not seen any proof from anyone that the SEC is coming after James.