Spectracare, Inc.
Country not established
- Devices
- 1
What Spectracare, Inc. makes
Spectracare, Inc. manufactures the Dwyer Eye Systems Aspiration Unit, a device designed for ophthalmic surgical procedures to remove fluids or debris from the eye during surgery.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dwyer Eye Systems Aspiration Unit Ref K913261
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spectracare, Inc. have in the registry?
The registry currently lists 1 device for Spectracare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spectracare, Inc.'s devices?
Among its 1 most recently registered device, Spectracare, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Spectracare, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Spectracare, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spectracare, Inc. in the registry?
The most recently registered devices listed for Spectracare, Inc. include DWYER EYE SYSTEMS ASPIRATION UNIT.