Precident Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Precident Corp. makes
Precident Corp. manufactures the FLUX-N-ALL, a device designed for medical imaging or alignment applications, and the PDI Parallel Sided Post Kit, a surgical or positioning accessory used in orthopedic or spinal procedures.
The company’s portfolio includes Class I and Class II devices, with products listed under the FDA’s 510(k) clearance pathway. Precident Corp. is based in the United States.
Catalogue
Flux-N-All Ref K911323
Regimes: 510(k) Registry: 510(k)Pdi Parallel Sided Post Kit Ref K913019
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precident Corp. have in the registry?
The registry currently lists 2 devices for Precident Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precident Corp.'s devices?
Among its 2 most recently registered devices, Precident Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Precident Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Precident Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precident Corp. in the registry?
The most recently registered devices listed for Precident Corp. include FLUX-N-ALL and PDI PARALLEL SIDED POST KIT.