FDA applicant

Multi-Channel Epilator

Sun Valley, CA1 decision1986–19860 recalls

FDA records 1 decision for Multi-Channel Epilator (Sun Valley, CA) in 1986: 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 Multi-Channel Epilator’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Multi-Channel Epilator since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Multi-Channel”

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

Multi-Med, Inc. 8 Multi Radiance Medical 3 Multi Biosensors, Inc. 2 Multi M Intl., Inc. 2 Multi Trading Corp. of America, Inc. 1 Multi-Com Sdn Bhd 1 Multi-Dimensional Imaging, Inc. 1 Multi-Spectrum Consulting, Inc. 1 Multi-Wash Medical, Ltd. 1 Multi Media Dental Systems, Inc. 1

Multi-Channel Epilator

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Multi-Channel”