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Facebow

ORMCO CORPORATION · Model 617-1015 · UDI-DI 00889989079869

DZB Prescription
10
510(k) clearances
17
Adverse events
0
Recalls
27
Facilities

Description

Facebow ,SHRT OB,STD SH IB,045

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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.