Home › SONTEC INSTRUMENTS, INC. › Wire/Pin Cutter
Wire/Pin Cutter
SONTEC INSTRUMENTS, INC. · Model 1100-530Q · UDI-DI 00192896109933
HXZ
Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities
Description
Wire/Pin Cutter Double Action Tungsten Carbide Angled Up Quantum
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.