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FDA PRODUCT CODE · CLASS II

QPB — System, Suction, Lipoplasty For Removal

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

DEVICE CLASS
Class II
REGULATION
21 CFR 878.5040
MEDICAL SPECIALTY
General, Plastic Surgery
REVIEW PANEL
SU
— Implant— Life-sustaining— GMP-exempt— Third-party review eligible
7
510(K)/PMA CLEARANCES
510k: 7
0
RECALL ENTRIES

Recent clearances

K251944Lipocosm, LLC · 510k2026-06-08
K253396Apyx Medical Corporation · 510k2026-05-08
K252495Newpong Co., Ltd. · 510k2026-04-03
K244050Apyx Medical Corporation · 510k2025-05-12
K244026Microaire Surgical Instruments, LLC · 510k2025-04-25
K242804Microaire Surgical Instruments, LLC · 510k2024-12-30
K241835Cellmyx · 510k2024-11-27

Related on SPEQ

Medical devices industry →Medical device quality (ISO 13485) →FDA device clearances →FDA enforcement & recalls →

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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