Regtec
Country not established
- Devices
- 1
What Regtec makes
Regtec manufactures the FRITCH Ophthalmic Endoscope, a device designed for internal examination of the eye, including structures like the retina and anterior chamber.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA 510(k) clearance registry. Regtec is based in the United States.
Catalogue
Fritch Ophthalmic Endoscope Ref K855151
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regtec have in the registry?
The registry currently lists 1 device for Regtec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regtec's devices?
Among its 1 most recently registered device, Regtec has devices listed in FDA 510(k) (1 device).
What risk classes do Regtec's devices fall under?
Among its 1 most recently registered device, the classes recorded for Regtec's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Regtec in the registry?
The most recently registered devices listed for Regtec include FRITCH OPHTHALMIC ENDOSCOPE.