Visual Diagnostics, Inc.
Country not established
- Devices
- 1
What Visual Diagnostics, Inc. makes
Visual Diagnostics, Inc. manufactures the THABEST-IGE, a diagnostic device designed for imaging or analysis of specific biological samples, likely related to allergy testing or immunology assessments.
The company’s portfolio is regulated under FDA’s Class II device classification, with the THABEST-IGE authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Thabest-Ige Ref K855053
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Visual Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Visual Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Visual Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Visual Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Visual Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Visual Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Visual Diagnostics, Inc. in the registry?
The most recently registered devices listed for Visual Diagnostics, Inc. include THABEST-IGE.