Suntech USA, Inc.
Country not established
- Devices
- 1
What Suntech USA, Inc. makes
Suntech USA, Inc. manufactures Suntech Model 3001 AllStar and Model 3401 Galaxy, which are electrical stimulation devices used for muscle re-education and rehabilitation in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Suntech Models 3001 Allstar & 3401 Galaxy Ref K850660
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Suntech USA, Inc. have in the registry?
The registry currently lists 1 device for Suntech USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suntech USA, Inc.'s devices?
Among its 1 most recently registered device, Suntech USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Suntech USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Suntech USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Suntech USA, Inc. in the registry?
The most recently registered devices listed for Suntech USA, Inc. include SUNTECH MODELS 3001 ALLSTAR & 3401 GALAXY.