FDA Registration Active 🇺🇸 United States

ADVANCE-ESTHETIC LLC

Reg #: 3013397886 · FEI: 3013397886 · Expires 2026
Products
10
Proprietary Names
49
Establishment Types
3
Classifications
10

Registration Details

Registration Name
ADVANCE-ESTHETIC LLC
Registration Number
3013397886
FEI Number
3013397886
Status
Active
Expiry Year
2026
Initial Importer
Yes
Address
4101 Ravenswood Rd Ste 110
City
Fort Lauderdale
State
FL
ZIP
33312
Country
US

Regulatory Submissions

510(k) Number
K212978

Owner / Operator

Firm Name
Advance-Esthetic LLC
Operator Number
10053538
Address
4101 Ravenswood Rd unit 121-123
City
Fort Lauderdale
State
FL
Postal Code
33312
Country
US
Correspondent
Kostiantyn Suichmez

Products

Device Name Product Code
Powered Laser Surgical Instrument GEX
Device, Pressure Applying KNM
Light, Wood'S, Fluorescence GMB
Massager, Therapeutic, Electric ISA
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect ONF
Device, Skin Potential Measurement HCJ
Over-The-Counter Powered Light Based Laser For Acne OLP
Light Based Over The Counter Wrinkle Reduction OHS
Lamp, Infrared, Therapeutic Heating ILY
Brush, Dermabrasion, Powered GFE

Proprietary Names

Zemits Quidion DUO Zemits Quidion Lite Zemits Quidion Zemits Erase ND Zemits PressMio Zemits DioPulse Zemits DetektiLight Zemits Demeter Zemits WaveRestore Zemits LipoPremo Zemits Abigon Zemits ColdRestore Zemits EndoLuxx Zemits Bionexis Zemits CelluGlide Zemits Leger Zemits Klein RF Zemits Sisley Zemits CrystalFrax Zemits FrioLift Zemits CelluSpice Zemits AknoEvit Zemits VivoTite Zemits DuoCratus Zemits DuoCratus Pro Zemits CarbonFrax Zemits IPL Light Expert 2 Zemits LumaGenix Zemits Skin Analysis System Zemits VeraFace Zemits LED Zemits YAGenix Zemits ExfoMatte Zemits CellTite Zemits Skin Expert Zemits OxiVelour Zemits HydroVerstand Zemits Klein El Zemits Verstand Zemits SonoSilk Zemits Adrinox 2 Zemits DermeLuxx Pro Zemits Verstand HD Zemits JoliPeel VivaFacial Platform Zemits Eau Sante Zemits Ultraglow Zemits Meister HydroDiamond Facial Platform

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility