LIPOSAVER LS-2000 by INEX International. Professional Medical Use Only FDA Class: II Medical Device. 510k-Cleared # 212969 Condition: New FDA Clearance: Not listed Availability: In Stock (Verification Required) Use Setting: Clinical / In-Office Use Only System Overview: The LIPOSAVER LS-2000 is an ultrasound-based fat emulsification system used in liposuction and body contouring procedures. The device delivers ultrasound energy through an interchangeable probe into tumescent fluid infiltrated in the treatment area. This action generates micro-bubbles between fat cells; as the bubbles expand and implode, adipocyte membranes are selectively disrupted while denser structures such as blood vessels, nerves, and fibrous connective tissue are largely spared. The emulsified fat mixes with the tumescent fluid for subsequent aspiration. The system offers two operation modes — continuous (N Mode) and pulsed (Z Mode, 50% duty ratio) — and supports probes of varying diameters (Φ1.2mm to Φ4.0mm) for use across tissue types ranging from soft to fibrous, and across body areas including the face, chin, arms, abdomen, flanks, back, calves, thighs, and buttocks. The handpiece and cable are autoclavable for reprocessing between procedures, and the system is operated via a touch-screen interface with dual foot pedal control. LIPOSAVER LS-2000 Core Technologies & Innovations Ultrasound Cavitation (Bubble Effect) Emulsification: Probe emits ultrasound energy into infiltrated tumescent fluid, generating micro-bubbles between fat cells that expand and implode, mechanically disrupting adipocyte membranes while largely sparing vasculature, nerves, and fibrous connective tissue Dual Operation Modes: N Mode delivers continuous ultrasound output; Z Mode delivers pulsed output at a 50% duty ratio Interchangeable Probe Diameters: Φ1.9mm, Φ2.9mm, and Φ3.7mm probes included as standard, with Φ1.2mm and Φ4.0mm probes available as optional accessories, for use across varying tissue densities and treatment areas Adjustable Acoustic Output: Output acoustic power range of 0–90W (±20%) at a probe operating frequency of 35–40kHz Autoclavable Handpiece and Cable: Handpiece and cable assembly are autoclave-sterilizable for reprocessing between procedures Dual Foot Pedal Control: Intraoperative activation of output modes via a dual foot controller Clinical Applications Ultrasound-assisted lipoplasty / fat emulsification Body contouring across soft and fibrous tissue types Skin retraction in the treated area following fat reduction All AeonEx clinical devices come with US-based training and technical/services support. Indications are provided for product identification only. AeonEx does not verify, endorse, or make clinical, medical, therapeutic, aesthetic, or performance claims for this product. Technical Specifications Specification Value Device name LIPOSAVER LS-2000 FDA Status 510k-Cleared # 212969 Classification Class II Medical Device Product technology Ultrasound-assisted liposuction (UAL) device Specific technology Ultrasound cavitation ("Bubble Effect") emulsification, 35–40kHz probe operating frequency Indications Ultrasound-assisted lipoplasty / fat emulsification; body contouring; skin retraction Power Output acoustic power 0–90W max (±20%) Spot size Not listed Device color options Not listed Device dimensions in inches 15.6" x 6.7" x 10.8" (W x H x L, converted from 396 x 170 x 275mm) Device weight in lbs 9.5 lbs (converted from 4.3 kg) Cooling type Not listed Graphic user interface type TFT touch-screen Graphic user interface size Not listed Is the device treatment customizable? Yes — 2 operation modes (N Mode: continuous output; Z Mode: pulsed output, 50% duty ratio); 5 interchangeable probe diameters (Φ1.2/1.9/2.9/3.7/4.0mm) Probe turning frequency 35kHz–40kHz Input power AC 100V–240V, 50–60Hz Operating temperature 10 to 40°C (50 to 104°F) Operating humidity 15% to 80% relative humidity, non-condensing Atmospheric pressure 79.051kPa to 101.325kPa Content type Product Clinical setting Clinic only Medical Segment Aesthetics Professional Regulatory Notice & Restricted Device Statement RESTRICTED DEVICE: This device is a professional-grade system. Per 21 CFR 801.109, sale is restricted to licensed healthcare practitioners or authorized clinical facilities. Licensure verification is mandatory prior to order fulfillment.
