Printerprezz
Country not established
- Devices
- 1
What Printerprezz makes
Printerprezz makes the GAIA Lumbar Interbody Fusion Device (LIFD) Family, which is a spinal implant used for lumbar interbody fusion procedures.
The GAIA Lumbar Interbody Fusion Device (LIFD) Family is classified as Class II and is listed in the FDA 510(k) registry; Printerprezz is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Printerprezz have in the registry?
The registry currently lists 1 device for Printerprezz. Devices recorded under merged duplicate company entries are counted once.
Which registries list Printerprezz's devices?
Among its 1 most recently registered device, Printerprezz has devices listed in FDA 510(k) (1 device).
What risk classes do Printerprezz's devices fall under?
Among its 1 most recently registered device, the classes recorded for Printerprezz's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Printerprezz in the registry?
The most recently registered devices listed for Printerprezz include GAIA Lumbar Interbody Fusion Device (LIFD) Family.