Skip to content

Bdf Plaza

Country not established

Devices
1

What Bdf Plaza makes

Bdf Plaza manufactures the B-WRAP, a medical device designed for vascular applications, likely intended for temporary or emergency circulatory support by wrapping around blood vessels to maintain patency or control bleeding.

The B-WRAP is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the U.S. regulatory database. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • B-Wrap Ref K863777

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

Frequently asked questions

How many devices does Bdf Plaza have in the registry?

The registry currently lists 1 device for Bdf Plaza. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bdf Plaza's devices?

Among its 1 most recently registered device, Bdf Plaza has devices listed in FDA 510(k) (1 device).

What are the newest devices from Bdf Plaza in the registry?

The most recently registered devices listed for Bdf Plaza include B-WRAP.

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