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Dbmedx, Inc.

United Statesfrom the FDA registration address FDA FEI 3008321254

Dbmedx, Inc. is a medical device manufacturer, with 6 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 14 Nov 2026.

Devices
6
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 5
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 5
  • FDA Class I 1
Identifiers
  • FDA FEI 3008321254
  • DUNS 827456927

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue6

Newest first, rows 1-6 of 6

Company details

FDA FEI number
3008321254
DUNS number
827456927
Address
10394 W Chatfield Ave, Littleton, CO, 80127
Phone
720.515.6630

Frequently asked questions

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

The registry currently lists 6 devices for Dbmedx, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dbmedx, Inc.'s devices?

Among its 6 most recently registered devices, Dbmedx, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 6 most recently registered devices, the classes recorded for Dbmedx, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Dbmedx, Inc. include BBS Revolution™ PD-010-0002, dBsonx™ PD-040-0014, Attendant® Prodigy™ Bladder Scanner PD-010-0007 and BBS Revolution™ Rolling Stand PD-040-0046.

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