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Borvo Medical, Inc.

Country not established FDA FEI 3033728927

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Borvo Medical, Inc. makes

Borvo Medical, Inc. manufactures the Borvo EVAC System in two configurations: the Ergo and Classic versions. These devices are designed for manual evacuation of bodily fluids, such as urine or stool, in clinical settings, including patient care and medical procedures.

The Borvo EVAC System is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3033728927
Address
2500 Old Middlefield Way Ste E, Mountain View, CA, 94043

Frequently asked questions

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

The registry currently lists 1 device for Borvo Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Borvo Medical, Inc.'s devices?

Among its 1 most recently registered device, Borvo Medical, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Borvo Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Borvo Medical, Inc. include Borvo EVAC System (Ergo); Borvo EVAC System (Classic).

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