FDA applicant

Barton-Carey Medical Products Co.

Perrysburg, OH1 decision1986–19860 recalls

FDA records 1 decision for Barton-Carey Medical Products Co. (Perrysburg, OH) in 1986: 1 510(k) clearance. All are in product code DWL (Stocking, Medical Support (To Prevent Pooling…). 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 hospital panel, where it files most

How often FDA has decided Barton-Carey Medical Products Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Barton-Carey Medical Products Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Barton-Carey Medical Products 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 “Barton-Carey”

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

Barton Medical Corp. 1

Barton-Carey Medical Products Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Barton-Carey”