Pneuma Therapeutics, Inc.
United Statesfrom the FDA registration address FDA FEI 3045323840
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Pneuma Therapeutics, Inc. makes
Pneuma Therapeutics, Inc. manufactures the XChange Device and the XChange System.
These products are classified as Class II medical devices and are listed in the FDA 510(k) database, with the company based in the United States.
Catalogue
XChange Device, XChange System Ref K210112
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045323840
- Address
- 1253 Holmgrove Dr, San Marcos, CA, 92078
Frequently asked questions
How many devices does Pneuma Therapeutics, Inc. have in the registry?
The registry currently lists 1 device for Pneuma Therapeutics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pneuma Therapeutics, Inc.'s devices?
Among its 1 most recently registered device, Pneuma Therapeutics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pneuma Therapeutics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pneuma Therapeutics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pneuma Therapeutics, Inc. in the registry?
The most recently registered devices listed for Pneuma Therapeutics, Inc. include XChange Device, XChange System.