510(k) Report

FDA product code · General and plastic surgery

Suction Lipoplasty System For Removal And Transfer

QUBClass II21 CFR 878.5040510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

Removal and transfer/reimplantation of autologous adipose tissue without further manipulation for aesthetic body contouring

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, general and plastic surgery panel

Twenty years of QUB at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FIG. 1 — QUB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QUB? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 878.5040.