FDA applicant

Bcd Products, Inc.

Walker, MI2 decisions1982–19830 recalls

FDA records 2 decisions for Bcd Products, Inc. (Walker, MI) from 1982 to 1983: 2 510(k) clearances. Most are in product codes KXZ (System, Thermographic, Liquid Crystal, Powered…) and HQJ (Implant, Absorbable, (Scleral Buckling Methods)). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Bcd Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bcd Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Bcd Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?