FDA applicant

Surx, Inc.

Livermore, CA3 decisions2002–20020 recalls

FDA records 3 decisions for Surx, Inc. (Livermore, CA) in 2002: 3 510(k) clearances. All are in product code MUK (Electrosurgical Radiofrequency System, Stress…). Its devices cite 12 predicates, 3 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 Surx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Surx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Surx, 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

Surx, 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?