Xpress Bcd LLC
United Statesfrom the FDA registration address FDA establishment FEI 3026674642
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
XPress BCD Breast Compression Device Ref K163388
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3026674642
- Address
- 6024 White Flint Drive, Frederick, MD, 21702
Frequently asked questions
How many devices does XPRESS BCD LLC have in the registry?
The registry currently lists 5 devices for XPRESS BCD LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list XPRESS BCD LLC's devices?
Among its 5 most recently registered devices, XPRESS BCD LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do XPRESS BCD LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for XPRESS BCD LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from XPRESS BCD LLC in the registry?
The most recently registered devices listed for XPRESS BCD LLC include Xpress BCD LLC Pyramidal, Xpress BCD LLC Inner Pack, Xpress BCD LLC Spherical and Xpress BCD LLC Flat.