Luma Vision Limited
IrelandFDA applicant, unverified
- Devices
- 3
What Luma Vision Limited makes
Luma Vision Limited manufactures the VERAFEYE System, which includes the VERAFEYE Imaging Catheter and the VERAFEYE Imaging System. These devices are designed for intravascular imaging, enabling detailed visualization of blood vessels during coronary and peripheral procedures.
The VERAFEYE System is classified as Class II under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
VERAFEYE Imaging Catheter (VF-VIC-002) Ref K261849
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luma Vision Limited have in the registry?
The registry currently lists 3 devices for Luma Vision Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luma Vision Limited's devices?
Among its 3 most recently registered devices, Luma Vision Limited has devices listed in FDA 510(k) (3 devices).
What risk classes do Luma Vision Limited's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Luma Vision Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luma Vision Limited in the registry?
The most recently registered devices listed for Luma Vision Limited include VERAFEYE Imaging Catheter (VF-VIC-002), VERAFEYE Imaging and Guidance System (VF-VIS-002) and VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System.