Precimed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Precimed, Inc. makes
Precimed, Inc. manufactures orthopedic fixation systems, including the Precimed Cannulated Screw System and the Precimed Hip Screw System, designed for internal bone stabilization and fracture repair.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Precimed Cannulated Screw System Ref K050754
Regimes: 510(k) Registry: 510(k)Precimed Hip Screw System Ref K023851
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Precimed, Inc. have in the registry?
The registry currently lists 2 devices for Precimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Precimed, Inc.'s devices?
Among its 2 most recently registered devices, Precimed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Precimed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Precimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Precimed, Inc. in the registry?
The most recently registered devices listed for Precimed, Inc. include PRECIMED CANNULATED SCREW SYSTEM and PRECIMED HIP SCREW SYSTEM.