Home › devemed GmbH › devemed
devemed
devemed GmbH · Model 7310-50 F · UDI-DI 04061644038152
HXZ
Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities
Description
Wire cutter TC | 13.5 cm for soft wires up to 0.7 mm for hard wires up to 0.5 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.
