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VelaShape III System 120V, Packaged

SYNERON MEDICAL LTD · Model FG71201R · UDI-DI 07290109952437

NUV
1
510(k) clearances
10
Adverse events
0
Recalls
20
Facilities

Description

VelaShape III System 120V, Packaged

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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.