Is PEMF safe, and who should not use it?
These answers cover reported side effects, contraindications including pacemakers, pregnancy and seizure history, and BioReg's regulatory position. FDA registration is a facility and device listing, not clearance or approval, and the distinction is stated plainly. Written for anyone assessing whether PEMF is appropriate for them.
4 questions in Safety & Contraindications.
Is PEMF safe?
Yes, PEMF therapy is considered very safe when used as directed. It's non-invasive, drug-free, and has been used clinically for over 60 years with an excellent safety record. The electromagnetic fields are low in frequency and intensity. Contraindications apply: see "Who should not use PEMF?" below.
Who this is for: Everyone considering PEMF therapy
What are the side effects of PEMF therapy?
PEMF is generally well-tolerated with minimal side effects. Some users may experience temporary, mild effects that resolve within 24 hours: mild fatigue, slight warmth, or tingling during treatment. These typically diminish with continued use.
Who this is for: Those starting PEMF therapy
Who should not use PEMF?
Absolute contraindications include: pacemakers, insulin pumps, or implanted electronic devices; cochlear implants; and implanted defibrillators (electromagnetic fields can interfere with these devices). Relative contraindications requiring physician approval: pregnancy, active bleeding disorders, recent organ transplants (immunosuppression concerns), and uncontrolled epilepsy.
Who this is for: Those with medical devices or specific health conditions
What is BioReg's FDA status?
BioReg devices are FDA registered. Registration is a facility and product listing status, not a clearance or an approval, and is not a finding of safety or efficacy. The FDA has cleared specific PEMF devices for specific indications. In 1979, PEMF was approved for non-union bone fractures. Subsequent approvals include post-surgical pain/edema, muscle stimulation, and depression (transcranial magnetic stimulation). Clearance is device- and indication-specific, not blanket approval for all PEMF uses.
Who this is for: Those researching regulatory status
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