FDA applicant

Remington Products Company, LLC

Bridgeport, CT3 decisions1989–20010 recalls

FDA records 3 decisions for Remington Products Company, LLC (Bridgeport, CT) from 1989 to 2001: 3 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and LEJ (Booth, Sun Tan). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Remington Products Company, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Remington Products Company, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Remington Products Company, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Remington”

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

Remington Medical, Inc. 19

Remington Products Company, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Remington”