FDA Device Intelligence
HomeINTEGRA LIFESCIENCES PRODUCTION CORPORATION › Integra® Jarit®

Integra® Jarit®

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 360156 · UDI-DI 10381780196983

HNF Prescription
10
510(k) clearances
385
Adverse events
2
Recalls
265
Facilities

Description

Integra® Jarit® Eye Suture (Gradle) Scissors, Curved, Blunt Tips

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2024-09-17MicroSurgical Technology IncDue to pin coming off of handles.

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 docs
Data 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.