FDA Device Intelligence
Home › Jeil Medical Corporation › Leforte Neuro System Bone Plate

Leforte Neuro System Bone Plate

Jeil Medical Corporation · Model NL-ST-004 · UDI-DI 08809282812439

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

Query this across every FDA database — by API.

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

Get your free API keyRead the docs
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.