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ADVANCE-ESTHETIC LLC

Last updated September 17, 2026

Information

Device	Model / Reference	Registries	Class	Status
Zemits Klein RF	1	FDA UDI	Class I	Active
Zemits Adrinox	1	FDA UDI	Class I	Active
Zemits Abigon Pro	2	FDA UDI	Class I	Active
Zemits Leger	2	FDA UDI	Class I	Active
Zemits Bionexis Lite	2	FDA UDI	Class I	Active
Zemits Klein EL	1	FDA UDI	Class I	Active
Zemits JoliPeel	1	FDA UDI	Class I	Active
Zemits DuoCratus	1	FDA UDI	Class II	Active
Zemits HydroVerstand	1	FDA UDI	Class I	Active
Zemits Verstand HD	1	FDA UDI	Class I	Active
Zemits CoolRestore Elegance	1	FDA UDI	Class I	Active
Zemits CelluSpice Pro	1	FDA UDI	Class I	Active
Zemits FrioLift	2	FDA UDI	Class I	Active
Zemits OxiVelour	1	FDA UDI	Class I	Active
Zemits EndoLuxx	2	FDA UDI	Class I	Active
Zemits DermeLuxx	1	FDA UDI	Class I	Active
Zemits CrystalFrax	1	FDA UDI	Class I	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Oct 9, 2023	Z-0095-2024	—	open, classified	Advance-Esthetic LLC failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standards and certification. This Recall provides correction by the firm regarding Zemits NdPrime Yag Tattoo Removal Laser. The product requires update or is missing the following in part: remote interlock connector, safety interlocks, manual reset mechanism, beam attenuator, tests for determination of compliance, certification, class IV designation and warning, labels, and labeling.