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Ulthera, Inc. · Model UR-1 Rev. A · UDI-DI 00840763101169

FWY
4
510(k) clearances
20
Adverse events
0
Recalls
6
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.