Home › Dentatus AB › Profin
Profin
Dentatus AB · Model PDH/SK · UDI-DI 07350081494834
8
510(k) clearances
39
Adverse events
1
Recalls
267
Facilities
Description
Profin Hand Instrument with Assorted Lamineer Tips - Lamineer Tip Single Sided Diamond Coated, 1 of Each: LTA-75 and LTA-150
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-05-09 | Biomet 3i, Inc. | The drill malfunctions while in use. The drill has been observed to become lodged in the handle. |
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.