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Medi-Flex Hospital Products, Inc.

United StatesFDA applicant, unverified

Devices
13

What Medi-Flex Hospital Products, Inc. makes

Medi-Flex Hospital Products, Inc. manufactures single-use medical accessories for wound care, intravenous (IV) site preparation, and catheter management. Products include adhesive removers for secure dressings, IV prep kits with antiseptic solutions, tracheostomy care kits, and occlusive dressings for central venous catheters. The company also supplies occlusive dressings for PICC lines and port-a-cath access kits, along with specialized applicators for skin preparation.

The portfolio comprises Class I, Class II, and unclassified devices, with most products listed via the FDA’s 510(k) pathway. These devices are regulated under U.S. federal law and appear in the FDA’s 510(k) clearance database. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Medi-Flex Hospital Products, Inc. have in the registry?

The registry currently lists 13 devices for Medi-Flex Hospital Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medi-Flex Hospital Products, Inc.'s devices?

Among its 13 most recently registered devices, Medi-Flex Hospital Products, Inc. has devices listed in FDA 510(k) (13 devices).

What risk classes do Medi-Flex Hospital Products, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Medi-Flex Hospital Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medi-Flex Hospital Products, Inc. in the registry?

The most recently registered devices listed for Medi-Flex Hospital Products, Inc. include SEPP ADHESIVE REMOVER, CEPTI-SEAL I.V. PREP KIT, TRACHEOSTOMY CARE KIT and K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH.

Generated automatically from registry data and not verified by a human reviewer.