Spectra-Shield, Inc.
Country not established
- Devices
- 1
What Spectra-Shield, Inc. makes
Spectra-Shield, Inc. manufactures the HUMAN II LENS, a device designed for ocular applications.
The HUMAN II LENS is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Human Ii Lens Ref K781927
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectra-Shield, Inc. have in the registry?
The registry currently lists 1 device for Spectra-Shield, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectra-Shield, Inc.'s devices?
Among its 1 most recently registered device, Spectra-Shield, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Spectra-Shield, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Spectra-Shield, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Spectra-Shield, Inc. in the registry?
The most recently registered devices listed for Spectra-Shield, Inc. include HUMAN II LENS.