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BENCOX DA Instruments Hip System
Corentec Co., Ltd · Model HA.0B2.0004 · UDI-DI 08800017285429
HTH
Prescription
3
510(k) clearances
0
Adverse events
0
Recalls
13
Facilities
Description
Anteversion Guide-Anterior Direction
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.