Home › INTEGRA LIFESCIENCES PRODUCTION CORPORATION › Integra® Jarit®
Integra® Jarit®
INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 405111 · UDI-DI 10381780198949
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities
Description
Integra® Gruenwald Nasal Forceps, 4-1/2", Thru-Cutting Jaws, 3.5mm x 11.3mm Jaw
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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.