Solana, Inc.
Country not established
- Devices
- 1
What Solana, Inc. makes
Solana, Inc. manufactures the SUNFLOWER, a medical device designed for [specific clinical purpose not provided; assume functional intent based on name—e.g., a surgical or diagnostic tool for vascular or ophthalmic applications, pending exact details].
The SUNFLOWER is classified as a Class II device under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Sunflower Ref K820123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Solana, Inc. have in the registry?
The registry currently lists 1 device for Solana, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Solana, Inc.'s devices?
Among its 1 most recently registered device, Solana, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Solana, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Solana, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Solana, Inc. in the registry?
The most recently registered devices listed for Solana, Inc. include SUNFLOWER.