510(k) Report

FDA applicant

American Hair Removal System Co.

Southern Pines, NC1 decision1990–19900 recalls

FDA records 1 decision for American Hair Removal System Co. (Southern Pines, NC) in 1990: 1 510(k) clearance. All are in product code KCX (Epilator, High Frequency, Tweezer-Type). 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 American Hair Removal System Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Hair Removal System Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — American Hair Removal System Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like American Hair Removal System Co.’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?

  • KCXEpilator, High Frequency, Tweezer-Type1decision

Who builds on its devices?

Later devices cite its devices 2 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.

  • K892514Ahrs Epilator 629American Hair Removal System Co. · 19902cite it

What has FDA decided for it lately?

  • K892514Ahrs Epilator 629American Hair Removal System Co. · 1990

The one decision as American Hair Removal System Co. →