Parallax Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Parallax Cranioset Ref K994022
Regimes: 510(k) Registry: 510(k)Parallax Tracer Radiopaque Particles Ref K991893
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Tracers Bone Cement Opacifier Ref K023445
Regimes: 510(k) Registry: 510(k)Tracers Ta Bone Cement Opacifier, Model Tcr-Ta Ref K033230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Parallax Medical, Inc. have in the registry?
The registry currently lists 6 devices for Parallax Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Parallax Medical, Inc.'s devices?
Among its 6 most recently registered devices, Parallax Medical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Parallax Medical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Parallax Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Parallax Medical, Inc. in the registry?
The most recently registered devices listed for Parallax Medical, Inc. include CLEARVIEW PLUS BONE AND VERTEBRAL BODY BIOPSY NEEDLES, PARALLAX CRANIOSET, PARALLAX TRACER RADIOPAQUE PARTICLES and PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES.