Silver Creek, Inc.
Country not established
- Devices
- 1
What Silver Creek, Inc. makes
Silver Creek, Inc. manufactures the LASEAWAY Alexandrite Laser System, a medical device designed for laser-based treatments.
The device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Laseaway Alexandrite Laser System Ref K982316
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Silver Creek, Inc. have in the registry?
The registry currently lists 1 device for Silver Creek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Silver Creek, Inc.'s devices?
Among its 1 most recently registered device, Silver Creek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Silver Creek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Silver Creek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Silver Creek, Inc. in the registry?
The most recently registered devices listed for Silver Creek, Inc. include LASEAWAY ALEXANDRITE LASER SYSTEM.