Porta Ray, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Porta Ray, Inc. makes
Porta Ray, Inc. makes the PIXIE, BETA I & BETA II, ALPHA I AND ALPHA II, and PORTA RAY MODEL 325 devices.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Pixie Ref K792665
Regimes: 510(k) Registry: 510(k)Beta I & Beta Ii Ref K811082
Regimes: 510(k) Registry: 510(k)Alpha I And Alpha Ii Ref K810276
Regimes: 510(k) Registry: 510(k)Porta Ray Model 325 Ref K864339
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Porta Ray, Inc. have in the registry?
The registry currently lists 4 devices for Porta Ray, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Porta Ray, Inc.'s devices?
Among its 4 most recently registered devices, Porta Ray, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Porta Ray, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Porta Ray, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Porta Ray, Inc. in the registry?
The most recently registered devices listed for Porta Ray, Inc. include PIXIE, BETA I & BETA II, ALPHA I AND ALPHA II and PORTA RAY MODEL 325.