FDA applicant

Klh Medical, Inc.

Houston, TX3 decisions1989–19920 recalls

FDA records 3 decisions for Klh Medical, Inc. (Houston, TX) from 1989 to 1992: 3 510(k) clearances. All are in product code 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Klh Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Klh Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?