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Integra® Miltex®

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 19-2116 · UDI-DI 10381780419082

KAE Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

Integra® Miltex® Goodhill Ear Forceps 3-3/8" Shaft, Cross-Serrated Jaws 5.5mm

Recalls

DateFirmReason
2025-01-31Aesculap IncThe forceps have been used in ways not covered by the design resulting in breakage of the clamps.

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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.