Sol Weiss MD, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Sol Weiss MD, Inc. makes
Sol Weiss MD, Inc. makes ophthalmic diagnostic devices, including the NU-SPEC D and GLO-SPEC series (I, II, and III), which are used for corneal topography and anterior segment imaging.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Nu-Spec D Ref K012859
Regimes: 510(k) Registry: 510(k)Glo-Spec Ref K013817
Regimes: 510(k) Registry: 510(k)Glo-Spec I, Ii And Iii Ref K020959
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sol Weiss MD, Inc. have in the registry?
The registry currently lists 3 devices for Sol Weiss MD, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sol Weiss MD, Inc.'s devices?
Among its 3 most recently registered devices, Sol Weiss MD, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Sol Weiss MD, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Sol Weiss MD, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sol Weiss MD, Inc. in the registry?
The most recently registered devices listed for Sol Weiss MD, Inc. include NU-SPEC D, GLO-SPEC and GLO-SPEC I, II AND III.