V-FC Pro Full
VIORA LTD · Model VTL48015-F · UDI-DI 07290016746785
PBX
Prescription
1
510(k) clearances
63
Adverse events
1
Recalls
74
Facilities
Description
Kit of V-FC Pro Handpiece, V-FC Pro Tips and maintenance kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-07-13 | Bios S.r.l. | In some systems, the unit continues to emit RF energy after the PAUSE button is pressed. |
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.
