Gryphus Diagnostics, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Gryphus Diagnostics, LLC makes
Gryphus Diagnostics, LLC produces modifications and variants of the BVBLUE device, a diagnostic tool designed for specific medical imaging applications.
The company’s portfolio is regulated under Class I medical devices in the U.S. and is listed via FDA 510(k) clearance. The company is based in the United States.
Catalogue
Modification To Bvblue Ref K050755
Regimes: 510(k) Registry: 510(k)Bvblue Ref K993732
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gryphus Diagnostics, LLC have in the registry?
The registry currently lists 2 devices for Gryphus Diagnostics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gryphus Diagnostics, LLC's devices?
Among its 2 most recently registered devices, Gryphus Diagnostics, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Gryphus Diagnostics, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gryphus Diagnostics, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gryphus Diagnostics, LLC in the registry?
The most recently registered devices listed for Gryphus Diagnostics, LLC include MODIFICATION TO BVBLUE and BVBLUE.