FDA Device Intelligence
Home › INTEGRA LIFESCIENCES PRODUCTION CORPORATION › Integra® Ruggles®-Redmond™

Integra® Ruggles®-Redmond™

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model R3325 · UDI-DI 10381780224501

HXZ Prescription
1
510(k) clearances
513
Adverse events
1
Recalls
247
Facilities

Description

Integra® Ruggles®-Redmond™ Hercules Supercutter, 8-1/2", 3mm Maximum Capacity, Tungsten Carbide

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.