Home › SONTEC INSTRUMENTS, INC. › MCGEE WIRE CLOSURE FORCEPS
MCGEE WIRE CLOSURE FORCEPS
SONTEC INSTRUMENTS, INC. · Model 469-120 · UDI-DI 00192896041783
HXP
Prescription
5
510(k) clearances
160
Adverse events
1
Recalls
158
Facilities
Description
MCGEE WIRE CLOSURE FORCEPS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-06-22 | Synthes USA HQ, Inc. | A complaint was received of the tips of the Matrix 5.5.mm Left and Right Coronal Bender breaking while bending a spinal rod component of the Matrix System. |
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.