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Tecomet

TECOMET INC. · Model AR-8956-10 · UDI-DI 00841435122062

HXZ Prescription
1
510(k) clearances
514
Adverse events
1
Recalls
247
Facilities

Description

Wire Cutter, 7" Safety Inserts, Front

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.