510(k) Report

FDA applicant

Lipose Corp.

Santa Barbara, CA2 decisions2008–20090 recalls

FDA records 2 decisions for Lipose Corp. (Santa Barbara, CA) from 2008 to 2009: 2 510(k) clearances. Most are in product codes QPB (System, Suction, Lipoplasty For Removal) and MUU (System, Suction, Lipoplasty). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Lipose Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2008: 12009: 1
2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Lipose Corp. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Lipose Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • QPBSystem, Suction, Lipoplasty For Removal1decision
  • MUUSystem, Suction, Lipoplasty1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 4 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K081848Lipose Fat Transfer SystemLipose Corp. · 20084cite it

What has FDA decided for it lately?

  • K093067Lipose Disposable CannulaLipose Corp. · 2009
  • K081848Lipose Fat Transfer SystemLipose Corp. · 2008

All 2 as Lipose Corp. →