Soring GmbH Sonoca Lipo

FDA 510(k) K052183 · Soring GmbH Medizintechnik

Substantially Equivalent

510(k) numberK052183

Submission

Device name
Soring GmbH Sonoca Lipo
Applicant
Soring GmbH Medizintechnik
Denton, TX, US
Received
August 10, 2005
Decision date
October 7, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
QPB – System, Suction, Lipoplasty For Removal
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5040
Specialty
General, Plastic Surgery

A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring

Other 510(k)s with product code QPB

510(k)DeviceApplicantDecision
K254135LipoSurg ARTISTQPB · Traditional Nouvag AG09/05/2026SE
K261710AYON™ Power Liposuction Cannulas and AYON™ Power Liposuction Cannula AdaptorsQPB · Traditional Apyx Medical Corporation08/21/2026SE
K251944Lipocosm Harmonic SystemQPB · Traditional Lipocosm, LLC06/08/2026SE
K253396AYON Body Contouring System™ (AYON SYSTEM)QPB · Traditional Apyx Medical Corporation05/08/2026SE
K252495Lssa (NP-200)QPB · Traditional Newpong Co., Ltd.04/03/2026SE
K244050AYON Body Contouring System (AYON SYSTEM)QPB · Traditional Apyx Medical Corporation05/12/2025SE
K244026PAL 7020 ConsoleQPB · Traditional Microaire Surgical Instruments, LLC04/25/2025SE
K242804PAL Aspiration SystemQPB · Traditional Microaire Surgical Instruments, LLC12/30/2024SE
K241835AirSculpt Body Contouring System (AIRS-1-SYS)QPB · Traditional Cellmyx11/27/2024SE
K240188Vitruvian LiposaberQPB · Traditional Black & Black Surgical, Inc.09/13/2024SE

More from Black & Black Surgical, Inc.

510(k)DeviceDecision
K093511Soring MBC200/BCC140GEI · Traditional 04/16/2010SE
K030028CPC by Soring GmbHGEI · Special 01/17/2003SE
K024059MBC SeriesGEI · Special 01/08/2003SE
K012753Soring GmbH Sonoca 180/190LFL · Traditional 11/13/2001SE
K993265Soring GmbH, Arco 3000, Arco 2000, Arco 1000, MBC 601, MBC 600GEI · Special 10/22/1999SE
K992026Soring GmbH, Sonoca 300BTA · Traditional 09/23/1999SE

Questions and answers

When was Soring GmbH Sonoca Lipo cleared by the FDA?

Soring GmbH Sonoca Lipo (K052183) received a 510(k) decision of Substantially Equivalent on October 7, 2005, 58 days after the submission was received.

What is the product code of K052183?

The FDA product code is QPB – System, Suction, Lipoplasty For Removal, a Class II (moderate risk) device regulated under 21 CFR 878.5040.