Gte Sylvania, Inc.
Country not established
- Devices
- 1
What Gte Sylvania, Inc. makes
Gte Sylvania, Inc. manufactures ACTIVATOR LIGHT, a device designed to provide targeted illumination for medical or procedural applications, such as wound care or surgical assistance.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Activator Light Ref K770215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gte Sylvania, Inc. have in the registry?
The registry currently lists 1 device for Gte Sylvania, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gte Sylvania, Inc.'s devices?
Among its 1 most recently registered device, Gte Sylvania, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gte Sylvania, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gte Sylvania, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gte Sylvania, Inc. in the registry?
The most recently registered devices listed for Gte Sylvania, Inc. include ACTIVATOR LIGHT.