FDA applicant

Medtexx Partners, Inc.

Crofton, MD1 decision1999–19990 recalls

FDA records 1 decision for Medtexx Partners, Inc. (Crofton, MD) in 1999: 1 510(k) clearance. 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 Medtexx Partners, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medtexx Partners, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medtexx Partners, 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 “Medtexx”

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

Medtexx Manufacturing Sdn. Bhd. 4 Medtexx Industries (Thai) Co., Ltd. 1

Medtexx Partners, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medtexx”