FDA applicant

Biosculpture Technology, Inc.

New York, NY1 decision2003–20030 recalls

FDA records 1 decision for Biosculpture Technology, Inc. (New York, NY) in 2003: 1 510(k) clearance. All are in product code QPB (System, Suction, Lipoplasty For Removal). 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 Biosculpture Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biosculpture Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Biosculpture Technology, 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

Biosculpture Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?