Phase I Corp.
Country not established
- Devices
- 1
What Phase I Corp. makes
Phase I Corp. manufactures the Phase I Curette, a surgical instrument designed for tissue removal procedures, including debridement and biopsy applications.
The Phase I Curette is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Phase I Curette Ref K935822
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phase I Corp. have in the registry?
The registry currently lists 1 device for Phase I Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phase I Corp.'s devices?
Among its 1 most recently registered device, Phase I Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Phase I Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Phase I Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phase I Corp. in the registry?
The most recently registered devices listed for Phase I Corp. include PHASE I CURETTE.