Invision Medical Technology
Also registered as InVision Medical Technology Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3042902406
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
InVision Precision Cardiac Amyloid Ref K243866
Regimes: 510(k) Registry: 510(k)InVision Precision LVEF (LVEF) Ref K232331
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3042902406
- Address
- 1497 Samedra St, Sunnyvale, CA, 94087
Frequently asked questions
How many devices does INVISION MEDICAL TECHNOLOGY have in the registry?
The registry currently lists 2 devices for INVISION MEDICAL TECHNOLOGY. Devices recorded under merged duplicate company entries are counted once.
Which registries list INVISION MEDICAL TECHNOLOGY's devices?
Among its 2 most recently registered devices, INVISION MEDICAL TECHNOLOGY has devices listed in FDA 510(k) (2 devices).
What risk classes do INVISION MEDICAL TECHNOLOGY's devices fall under?
Among its 2 most recently registered devices, the classes recorded for INVISION MEDICAL TECHNOLOGY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from INVISION MEDICAL TECHNOLOGY in the registry?
The most recently registered devices listed for INVISION MEDICAL TECHNOLOGY include InVision Precision Cardiac Amyloid and InVision Precision LVEF (LVEF).