QKLClass II

Lipoaspirate Washing System For Aesthetic Body Contouring

21 CFR 878.5040 / General, Plastic Surgery

QKL is the FDA product code for Lipoaspirate Washing System For Aesthetic Body Contouring, a class II device type, regulated under 21 CFR 878.5040. FDA's definition for this code reads: "Wash, filter, concentrate, and or fragment autologous adipose tissue aspirated via liposuction for aesthetic body contouring without further manipulation". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QKL
Device name: Lipoaspirate Washing System For Aesthetic Body Contouring
FDA definition: Wash, filter, concentrate, and or fragment autologous adipose tissue aspirated via liposuction for aesthetic body contouring without further manipulation
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: 0
Ingested recalls: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 26 companies shown, in name order

Recent clearances

Product code QKL

FDA records hold no clearances under product code QKL.

Recent recalls

Product code QKL

FDA records show no recalls under product code QKL.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)