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Leforte Neuro System Bone Plate

Jeil Medical Corporation · Model N16-MM-010F · UDI-DI 08809265156246

HBWGXRGWO Prescription
1
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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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.