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Tua

VUPIESSE SRL · Model Face Fitness · UDI-DI 08017129000912

NFO
1
510(k) clearances
37
Adverse events
2
Recalls
60
Facilities

Description

Facial stimulator indicated for over the counter cosmetic use.

Recalls

DateFirmReason
2012-01-06Ion Genius, Inc.Wires do not meet performance standards under 21 CFR 898 and have unprotected electrode configurations. Additionally, devices were sold/distributed without 510(k) or PMA
2012-01-06Ion Genius, Inc.Wires do not meet performance standards under 21 CFR 898 and have unprotected electrode configurations. Additionally, devices were sold/distributed without 510(k) or PMA

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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.