FDA applicant

Medi-Flex Hospital Products, Inc.

Overland Park, KS13 decisions1991–19970 recalls

FDA records 13 decisions for Medi-Flex Hospital Products, Inc. (Overland Park, KS) from 1991 to 1997: 13 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and FMF (Syringe, Piston). 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-Flex Hospital Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medi-Flex Hospital Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medi-Flex Hospital Products, 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-Flex”

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

Medi-Tech, Inc. 36 Medi-Globe Corp. 26 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 Tex, Inc. 4 Medi-Dose, Inc. 4 Medi-Source, Inc. 4

Medi-Flex Hospital Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medi-Flex”