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NA
Synthes GmbH · Model 443.172 · UDI-DI 10705034779928
NQW
Prescription
1
510(k) clearances
202
Adverse events
0
Recalls
71
Facilities
Description
2.0MM TI MINIPLATE-SINGLE BEND 35MM/12MM SPACING
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 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.
