Home › Device types › ILX
Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
FDA product code ILX · Class 2 · Physical Medicine
38
Registered devices
8
Adverse events
1
Recalls
15
510(k) clearances
Devices with this code
OrthoCor Medical — Caerus Corp.TrueStim — Hi-Dow International IncorporatedOrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.Disposable Applicator Cover — Regenesis Biomedical, Inc.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.TrueStim — Hi-Dow International IncorporatedOrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.Provant Infinity — Regenesis Biomedical, Inc.OrthoCor Medical — Caerus Corp.TrueStim — Hi-Dow International IncorporatedOrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.OrthoCor Medical — Caerus Corp.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-09-29 | Regenesis Biomedical Inc | In the course of device testing, the firm determined that the affected devices may, under certain unusual clinical circumstance, be unable to generate a therap |
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