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ORTHOFIX

ORTHOFIX SRL · Model 1 · UDI-DI 18059015373103

HSB
1
510(k) clearances
37,835
Adverse events (115 deaths)
0
Recalls
301
Facilities

Description

RODEO TELESCOPIC NAIL L140MM D3.5MM STERILE

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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.