Bioelectronics Corp (BIEL)

[Zorax]

The only link I need. And I already posted many examples. I can't make anyone follow the links.
But even though I admire all the effort to defend whelan and actipatch, if history proves itself correct again, with the heavy litigation and lawsuits against whelan and biel, the first thing that will be thrown under the bus will be bioelectronics corp and shareholders as whelan desperatly throws everything away to save his ass and his family's ass first and foremost.

But anyways, 318 results on the first try...I'm pretty sure a boatload of those are US fda approved.
https://www.amazon.com/s/ref=nb_sb_noss_1?url=search-alias%3Daps&field-keywords=pemf&rh=i%3Aaps%2Ck%3Apemf

http://www.accessdata.fda.gov/cdrh_docs/pdf15/K152432.pdf

Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in..

And this tells us it's not approved for sale in the us.
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Indications for Use
Form Approved: OMB No. 0910-0120
Expiration Date: January 31, 2017

biel was reclassified II in the hopes to market to the US, but biel didn't follow through with all the compliance. Simply, if biel was compliant in all rules and regs, they would already be in wall greens or whatever in the States.

from doc oz show years ago.. biel hasn't gotten any closer to the States. Why bother?
Oh wait, biel actipatch was a class II in Canada in 2011?

"PEMF Knee Device

Also on the show, family physician Dr. William Pawluk discussed the OrthoCor Active Knee System. This is an FDA-approved device that combines PEMF energy and thermal therapy to increase circulation and thus reduce swelling, relieve chronic pain and arthritis, as well as improve range of motion. The device’s technology consists of a cuff that surrounds the knee. It has a coil and heat pods that send magnetic pulses and heat through the injured tissue. Patients can walk while the OrthoCor device is in operation. OrthoCor sells its products through orthopedic clinics, physicians and health care practitioners.

PEMF Patch Devices

Dr. Pawluk also introduced a small, disposable PEMF device called Acti-Patch by Bioelectronics Corp. In Canada, ActiPatch is a Class II device and is sold over-the-counter. Health Canada has approved it for relief of musculoskeletal pain. It is not FDA-approved for musculoskeletal pain, so the efficacy of these patches is still unclear. It may have some benefit with superficial pain and edema."