510(k) Report

FDA applicant

Facemaster of Beverly Hills, Inc.

Irvine, CA1 decision2005–20050 recalls

FDA records 1 decision for Facemaster of Beverly Hills, Inc. (Irvine, CA) in 2005: 1 510(k) clearance. All are in product code NFO (Stimulator, Transcutaneous Electrical…). 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, neurology panel, where it files most

How often FDA has decided Facemaster of Beverly Hills, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Facemaster of Beverly Hills, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Facemaster of Beverly Hills, 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

Which product codes does it file in?

  • NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes1decision

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.

  • K040871Facemaster Facial Toning SystemFacemaster of Beverly Hills, Inc. · 20054cite it

What has FDA decided for it lately?

  • K040871Facemaster Facial Toning SystemFacemaster of Beverly Hills, Inc. · 2005

The one decision as Facemaster of Beverly Hills, Inc. →