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Mill-Tech Ent., Inc.

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Devices
1

What Mill-Tech Ent., Inc. makes

Mill-Tech Ent., Inc. manufactures the TOI-LIFT, a device designed for lifting and positioning patients in clinical or home care settings. This product is intended to assist healthcare providers in safely transferring individuals with limited mobility, reducing manual handling risks.

The TOI-LIFT is classified under Class I by the FDA and has been submitted for 510(k) clearance. The company is based in the United States, where its devices are subject to U.S. regulatory requirements.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Toi-Lift Ref K896814

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Mill-Tech Ent., Inc. have in the registry?

The registry currently lists 1 device for Mill-Tech Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.

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

Among its 1 most recently registered device, Mill-Tech Ent., Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Mill-Tech Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Mill-Tech Ent., Inc. in the registry?

The most recently registered devices listed for Mill-Tech Ent., Inc. include TOI-LIFT.

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