FDA applicant

Medmark, Inc.

Versailles, OH3 decisions1989–19910 recalls

FDA records 3 decisions for Medmark, Inc. (Versailles, OH) from 1989 to 1991: 3 510(k) clearances. Most are in product codes KFK (Saw, Pneumatically Powered) and LYY (Latex Patient Examination Glove). 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 Medmark, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medmark, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Medmark”

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

Medmark Technologies, LLC 1

Medmark, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medmark”