Pulmera, Inc.
United Statesfrom the FDA registration address FDA FEI 3049422862
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Pulmera, Inc. makes
Pulmera, Inc. manufactures the C-beam device, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
- Registry: GUDID
C-beam Ref K252735
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3049422862
- DUNS number
- 116814767
- Address
- 7th floor, 905 Pearl Parkway, Charlotte, NC, 28204
Frequently asked questions
How many devices does Pulmera, Inc. have in the registry?
The registry currently lists 2 devices for Pulmera, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pulmera, Inc.'s devices?
Among its 2 most recently registered devices, Pulmera, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pulmera, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pulmera, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pulmera, Inc. in the registry?
The most recently registered devices listed for Pulmera, Inc. include C-beam 1.0 and C-beam.