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Tecomet

TECOMET INC. · Model TM157065-AU · UDI-DI 00841435107656

HXX Prescription

510(k) clearances

23,582

Adverse events (4 deaths)

Recalls

466

Facilities

Description

TORQUE-LIMITING,STANDARD-T 3mm HEX MALE 65LBS.-IN. RED ORTHO-GRIP™

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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.