FDA applicant

Cytori Therapeutics, Inc.

San Diego, CA6 decisions2006–20140 recalls

FDA records 6 decisions for Cytori Therapeutics, Inc. (San Diego, CA) from 2006 to 2014: 6 510(k) clearances. Most are in product codes MUU (System, Suction, Lipoplasty) and CAC (Apparatus, Autotransfusion). Its devices cite 15 predicates, 4 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 Cytori Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2014

2007high 2 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cytori Therapeutics, Inc.’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

Cytori Therapeutics, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?