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AGILON® XO Goniometer

implantcast GmbH · Model 78013000 · UDI-DI 04048844381226

KQW
10
510(k) clearances
4
Adverse events
0
Recalls
81
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.