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Medi-Tech, Inc.

Also registered as Meditech, Meditech, Ltd.

Country not established

Devices
39

What Medi-Tech, Inc. makes

Medi-Tech, Inc. manufactures medical devices including external male nursing catheters, transluminal balloon catheters, enteric feeding tubes, and peripheral dilatation catheters. Their portfolio also covers diagnostic tools such as coagulation reference plasma, drug monitoring controls, and immunoassay calibrators. Surgical and interventional products include titanium Greenfield vena cava filter carriers, soft stents, polypectomy snares, and T-fasteners, along with modified labeling for granulated gel products.

The company’s devices are regulated under FDA Class I and Class II classifications, with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, and 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-Tech, Inc. have in the registry?

The registry currently lists 39 devices for Medi-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medi-Tech, Inc.'s devices?

Among its 39 most recently registered devices, Medi-Tech, Inc. has devices listed in FDA 510(k) (39 devices).

What risk classes do Medi-Tech, Inc.'s devices fall under?

Among its 39 most recently registered devices, the classes recorded for Medi-Tech, 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-Tech, Inc. in the registry?

The most recently registered devices listed for Medi-Tech, Inc. include HYPODERMIC NEEDLES & SYRINGES, MEDI-TECH DILATATION CATHETERS, CATHETER, EXTERNAL MALE NURSING CARE and CATHETER, TRANSLUMINAL BALLOON.

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