QPBClass II

System, Suction, Lipoplasty For Removal

21 CFR 878.5040 / General, Plastic Surgery

QPB is the FDA product code for System, Suction, Lipoplasty For Removal, a class II device type, regulated under 21 CFR 878.5040. FDA's definition for this code reads: "A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring". As of 2026-09-10, FDA records hold 59 510(k) clearances under this code, the most recent dated 2026-08-21, and one recall.

Classification record

Product code: QPB
Device name: System, Suction, Lipoplasty For Removal
FDA definition: A suction lipoplasty system is a device intended for the removal of adipose tissue for purposes of aesthetic body contouring
Regulation: 21 CFR 878.5040
Device class: Class II
Review panel: General, Plastic Surgery
Submission type: 510(k)
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 60
Ingested recalls: 1

Clearances, product code QPB

By decision year

60 clearances under product code QPB with a decision year between 1998 and 2026, 1998 the highest year at 6.

Show the numbers

510(k) clearances under FDA product code QPB by decision year
Year	Clearances
1998	6
1999	2
2000	2
2001	5
2002	1
2003	2
2004	2
2005	1
2006	2
2007	2
2008	4
2009	1
2010	2
2011	2
2012	3
2014	1
2015	1
2016	1
2017	3
2019	2
2020	2
2022	2
2024	4
2025	2
2026	5

Applicants with the most clearances

Product code QPB

Applicants holding the most 510(k) clearances under product code QPB
Applicant	Clearances
MicroAire Surgical Instruments, LLC	8
Solta Medical, Inc.	5
Black & Black Surgical, Inc.	3
Byron Medical	3
Andrew Technologies, LLC	2
Apyx Medical Corporation	2
Euromi S.A.	2
Lysonix, Inc.	2
Medela AG	2
Mentor	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 46 companies shown, in name order