FDA applicant

Stephens Mfg. Co.

Washington, DC1 decision1991–19910 recalls

FDA records 1 decision for Stephens Mfg. Co. (Washington, DC) in 1991: 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 Stephens Mfg. Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stephens Mfg. Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Stephens”

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

Stephens Instruments 5 Stephens Scientific 4

Stephens Mfg. Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Stephens”