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

Integra® Jarit®

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 275504 · UDI-DI 10381780185376

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
246
Facilities

Description

Integra® Jarit® Replacement Blade Kit, For REF# 275-503, Includes: 1-Pair T/C Blades, 4-Screws, 1-Hexagonal Key

Recalls

DateFirmReason
2020-11-20Zimmer 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 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.