Sabre-K, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Sabre-K, Ltd. makes
Sabre-K, Ltd. manufactures orthopedic fixation systems, including the KURER CROWN SAVER K4 ANCHOR SYSTEM (universal and ready-core kits) and the KURER FIN-LOC, which are designed for bone stabilization and fracture management.
These devices are classified as Class I under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sabre-K, Ltd. have in the registry?
The registry currently lists 1 device for Sabre-K, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sabre-K, Ltd.'s devices?
Among its 1 most recently registered device, Sabre-K, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sabre-K, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sabre-K, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sabre-K, Ltd. in the registry?
The most recently registered devices listed for Sabre-K, Ltd. include KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOC.