Skip to content

Bomdal Medical Equipment, Inc.

CanadaFDA applicant, unverified

Devices
2

What Bomdal Medical Equipment, Inc. makes

Bomdal Medical Equipment, Inc. manufactures patient transfer devices, including the BOMDAL STANDARD LIFT and BOMDAL TRAVELMASTER LIFT, designed for assisting healthcare providers in moving patients safely within clinical settings.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Bomdal Standard Lift Ref K862147

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bomdal Travelmaster Lift Ref K862146

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

Frequently asked questions

How many devices does Bomdal Medical Equipment, Inc. have in the registry?

The registry currently lists 2 devices for Bomdal Medical Equipment, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bomdal Medical Equipment, Inc.'s devices?

Among its 2 most recently registered devices, Bomdal Medical Equipment, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Bomdal Medical Equipment, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Bomdal Medical Equipment, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Bomdal Medical Equipment, Inc. in the registry?

The most recently registered devices listed for Bomdal Medical Equipment, Inc. include BOMDAL STANDARD LIFT and BOMDAL TRAVELMASTER LIFT.

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