510(k) Report

FDA applicant

Sound Surgical Technologies, LLC

Lafayette, CO6 decisions1999–20123 recalls

FDA records 6 decisions for Sound Surgical Technologies, LLC (Lafayette, CO) from 1999 to 2012: 6 510(k) clearances. Most are in product codes QPB (System, Suction, Lipoplasty For Removal) and LFL (Instrument, Ultrasonic Surgical). Its devices cite 15 predicates, 3 of them its own earlier devices. 3 recalls are 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 Sound Surgical Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2011: 22012: 1
2007high 2 (2011) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

1in 2017

2007: 12010: 12017: 1
2007high 1 (2007) · low 0 (2008)2026

Class I Class II/III not classified

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

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

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Other applicant names beginning “Sound”

FDA records each applicant name separately; these may or may not be the same firm.