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LB1 + LF1 kit

VENUS CONCEPT LTD · Model PK000041 · UDI-DI 07290016540079

PBXGEI Prescription
10
510(k) clearances
63
Adverse events
1
Recalls
75
Facilities

Description

Venus Legacy LB1 and LF1 applicators package for shipment

Recalls

DateFirmReason
2017-07-13Bios S.r.l.In some systems, the unit continues to emit RF energy after the PAUSE button is pressed.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.