Visionex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Visionex, Inc. makes
Visionex, Inc. manufactures a trabeculo-suprachoridal shunt for managing intraocular pressure in glaucoma patients and tear volume test devices for assessing ocular surface health.
The company’s portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance pathway. Visionex, Inc. is based in the United States.
Catalogue
Trabeculo-Suprachoroidal Shunt Ref K902296
Regimes: 510(k) Registry: 510(k)Tear Volume Tests Ref K881515
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visionex, Inc. have in the registry?
The registry currently lists 2 devices for Visionex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visionex, Inc.'s devices?
Among its 2 most recently registered devices, Visionex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Visionex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Visionex, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visionex, Inc. in the registry?
The most recently registered devices listed for Visionex, Inc. include TRABECULO-SUPRACHOROIDAL SHUNT and TEAR VOLUME TESTS.