Vee Gee Scientific, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Vee Gee Scientific, Inc. makes
Vee Gee Scientific, Inc. manufactures clinical refractometers, including models 3471, 2730, 2740, 2721, 3461, and A300CL. These devices measure refractive index and are used in clinical settings to assess tear film osmolarity, aiding in the diagnosis of dry eye syndrome.
The company’s refractometers are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The devices are based in the United States and appear in the FDA’s regulatory records.
Catalogue
Model 3471 Clinical Refractometer Ref K941902
Regimes: 510(k) Registry: 510(k)Model 2730 Clinical Refractometer Ref K941906
Regimes: 510(k) Registry: 510(k)Model 2740 Clinical Refractometer Ref K941903
Regimes: 510(k) Registry: 510(k)Model 2721 Clinical Refractometer Ref K941901
Regimes: 510(k) Registry: 510(k)Model 3461 Clinical Refractometer Ref K941905
Regimes: 510(k) Registry: 510(k)Model A300CL Clinical Refractometer Ref K941904
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vee Gee Scientific, Inc. have in the registry?
The registry currently lists 6 devices for Vee Gee Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vee Gee Scientific, Inc.'s devices?
Among its 6 most recently registered devices, Vee Gee Scientific, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Vee Gee Scientific, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Vee Gee Scientific, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vee Gee Scientific, Inc. in the registry?
The most recently registered devices listed for Vee Gee Scientific, Inc. include MODEL 3471 CLINICAL REFRACTOMETER, MODEL 2730 CLINICAL REFRACTOMETER, MODEL 2740 CLINICAL REFRACTOMETER and MODEL 2721 CLINICAL REFRACTOMETER.