FDA applicant

Medi Tex, Inc.

New York, NY4 decisions1984–19920 recalls

FDA records 4 decisions for Medi Tex, Inc. (New York, NY) from 1984 to 1992: 4 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and FMI (Needle, Hypodermic, Single Lumen). 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 Medi Tex, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medi Tex, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medi Tex, 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 “Medi”

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

Medi-Tech, Inc. 36 Medi-Globe Corp. 26 Medi-Flex Hospital Products, Inc. 13 Medi-Plast Intl., Inc. 12 The Medi-Dose Group 10 Medi Nuclear Corp., Inc. 9 Medi-Physics Inc. Dba Nycomed Amersham Imaging 9 Medi-Craft, Ltd. 9 Medi-Spec 8 Medi-Man Rehabilitation Products, Inc. 4 Medi-Dose, Inc. 4 Medi-Source, Inc. 4

Medi Tex, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medi”