Home › INTEGRA LIFESCIENCES PRODUCTION CORPORATION › Integra® Jarit®
Integra® Jarit®
INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 275500 · UDI-DI 10381780185338
HXZ
Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
246
Facilities
Description
Integra® Jarit® Hercules Supercutter, 8-3/4", 3mm Maximum, Angled 30°, Large
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.