Teleflex Medical Group
Country not established
- Devices
- 1
What Teleflex Medical Group makes
Teleflex Medical Group manufactures external fixation devices, including the KMEDIC system, used for stabilizing and supporting fractured bones through percutaneous pins and frames.
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
Kmedic External Fixation Devices Ref K030336
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teleflex Medical Group have in the registry?
The registry currently lists 1 device for Teleflex Medical Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teleflex Medical Group's devices?
Among its 1 most recently registered device, Teleflex Medical Group has devices listed in FDA 510(k) (1 device).
What risk classes do Teleflex Medical Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Teleflex Medical Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teleflex Medical Group in the registry?
The most recently registered devices listed for Teleflex Medical Group include KMEDIC EXTERNAL FIXATION DEVICES.