Orange-Sol, Inc.
Country not established
- Devices
- 1
What Orange-Sol, Inc. makes
Orange-Sol, Inc. manufactures the MEDI-SOL, a Class I medical device designed for [specific use not detailed in provided data].
The MEDI-SOL is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Medi-Sol Ref K924571
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orange-Sol, Inc. have in the registry?
The registry currently lists 1 device for Orange-Sol, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orange-Sol, Inc.'s devices?
Among its 1 most recently registered device, Orange-Sol, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orange-Sol, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orange-Sol, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Orange-Sol, Inc. in the registry?
The most recently registered devices listed for Orange-Sol, Inc. include MEDI-SOL.