510(k) Report

FDA applicant

Wahl Clipper Corp.

Steriling, IL8 decisions1994–19950 recalls

FDA records 8 decisions for Wahl Clipper Corp. (Steriling, IL) from 1994 to 1995: 8 510(k) clearances. Most are in product codes ISA (Massager, Therapeutic, Electric) and IRO (Vibrator, Therapeutic). 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, physical medicine panel, where it files most

How often FDA has decided Wahl Clipper Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Wahl Clipper Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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