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Bigliani/Flatow

Orthosoft Inc · Model 20-8075-007-02 · UDI-DI 00889024304161

PBF Prescription
1
510(k) clearances
226
Adverse events (1 deaths)
0
Recalls
35
Facilities

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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.