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OrthoCor Medical

Caerus Corp. · Model Activ8 Back - XS · UDI-DI 00851979007442

ILXIRT Prescription
1
510(k) clearances
8
Adverse events
1
Recalls
7
Facilities

Description

The Activ8 family of devices are portable, compact, lightweight, non-invasive system designed to deliver transcutaneous pulsed electromagnetic field (PEMF) stimulation therapy and electronic heat for adjunctive use in the temporary relief of pain, such as pain associated with over-exertion, strains, sprains, and arthritis.

Recalls

DateFirmReason
2008-09-29Regenesis Biomedical IncIn the course of device testing, the firm determined that the affected devices may, under certain unusual clinical circumstance, be unable to generate a therapeutic dose of radio

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.