Fda Approved Pemf Devices

In the usa none of the pemf devices including the curatron have been cleared approved or certified for use for general purpose health applications by the fda.

Fda approved pemf devices. In 2013 the fda approved pemf therapy for use in the treatment of migraine headaches. Some companies use words to make the reader believe that their device. On october 13th 2015 the fda reclassified pemf devices from their existing class 3 category to a class 2 status and most pemf devices that are sold today in the united states are fda. Bemer fda approval as commonly referred to online is actually what is known as an fda registration via the fda 510 k form.

On october 13th 2015 the fda reclassified pemf devices from their existing class 3 category to a class 2 status and most pemf devices that are sold today in the united states are fda registered as wellness devices. On the other hand fda approval needs to be earned by proving that a pemf device has health benefits that it can be used to treat a specific health condition and that the benefits outweigh possible risks. In 2006 the fda approved pemf therapy for treatment of depression and anxiety. In 2004 the fda approved pemf therapy for cervical fusion patients at high risk of non fusion.

Some devices are listed or registered as massage or biofeedback devices but none including the curatron are approved for general purpose health or pain relief. There are companies who mislead customers and tell them that their device has been fda. In 1998 the fda approved pemf therapy for urinary incontinence and muscle stimulation. Some devices are listed on the fda website as massage or biofeedback devices but no one is cleared approved or certified for pemf pain relief.

In 2006 the fda approved pemf therapy for treatment of depression and anxiety. Most often very high intensity pemf devices are fda approved such as the neurostar which can be used to fight depression. Surprisingly marketers and manufacturers have gone through pre market approval pma or 501 k submissions to market their pemf products and have been caught making false claims our goal is to expose the functionality of pemf devices. An fda 510 k form allows the fda to determine whether or not a device or product will fall into a category of devices which has already been reviewed by the fda and deemed either safe or unsafe.

In the usa no pemf machines have been cleared approved or certified for use for general purpose health applications by the usa food and drug administration.