Home › SOFWAVE MEDICAL LTD › Sofwave Applicator
Sofwave Applicator
SOFWAVE MEDICAL LTD · Model FG00003-R · UDI-DI 07290018152065
4
510(k) clearances
219
Adverse events
1
Recalls
17
Facilities
Description
This applicator is the refurbish version of the small (precise) applicator, designed to allow the user treatment flexibility and easier access to smaller and more curved areas.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-08-30 | RoyalVibe Health Ltd. | Ultrasound devices were not authorized, cleared, or approved by FDA, and thus their performance characteristics have not been adequately established. There is a possibility of cust |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
