Jovi, Inc.
Country not established
- Devices
- 1
What Jovi, Inc. makes
Jovi, Inc. manufactures the Jovi Myelography Harness, a device used in spinal imaging procedures to stabilize and position patients during myelography examinations.
The company’s portfolio is regulated under FDA Class II devices, with the Jovi Myelography Harness listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
Jovi Myelography Harness Ref K872468
510(k) 510(k)
Frequently asked questions
How many devices does Jovi, Inc. have in the registry?
The registry currently lists 1 device for Jovi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jovi, Inc.'s devices?
Among its 1 most recently registered device, Jovi, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jovi, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jovi, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jovi, Inc. in the registry?
The most recently registered devices listed for Jovi, Inc. include JOVI MYELOGRAPHY HARNESS.