Home › Gimmi GmbH › Gimmi
Gimmi
Gimmi GmbH · Model AA.1998.12 · UDI-DI 04049047006299
HXZ
Prescription
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities
Description
UNIVERSAL WIRE SCISSORS TC LENGTH 120 MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-11-20 | Zimmer Biomet, Inc. | Device has the potential for fracture during use. |
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.