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1.5/0.6MM

BIOMET MICROFIXATION, INC · Model SP-1658 · UDI-DI 00841036282240

HBWGXRJEYGWO Prescription
3
510(k) clearances
81
Adverse events
1
Recalls
35
Facilities

Recalls

DateFirmReason
2024-01-24Synthes (USA) Products LLCProducts not sterilized, sterility cannot be confirmed

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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.