FDA applicant

Associated Electrolysis Group

Mchenry, IL1 decision1980–19800 recalls

FDA records 1 decision for Associated Electrolysis Group (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code KCW (Epilator, High Frequency, Needle-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 Associated Electrolysis Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Associated Electrolysis Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Associated Electrolysis Group’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

Other applicant names beginning “Associated”

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

Associated Medical Products Co. 29 Associated Mills, Inc. 14 Associated Ent., Inc. 4 Associated Medical 3 Associated Electro-Medical Services, Inc. 2 Associated Medical Devices, Inc. 2 Associated Hospital Services, Inc. 1 Associated Premium Corp. 1 Associated Medical Representatives 1 Associated Hearing Instruments 1

Associated Electrolysis Group

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Associated”