Inter-Os Technologies
Country not established
- Devices
- 2
What Inter-Os Technologies makes
Inter-Os Technologies manufactures the INTER-OS Limb Lengthener, a device designed to adjust and extend limb length for patients requiring gradual elongation of bones.
The INTER-OS Limb Lengthener is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Inter-Os Bone Generator Ref K993869
Regimes: 510(k) Registry: 510(k)Inter-Os Limb Lengthener Ref K031875
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inter-Os Technologies have in the registry?
The registry currently lists 2 devices for Inter-Os Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inter-Os Technologies's devices?
Among its 2 most recently registered devices, Inter-Os Technologies has devices listed in FDA 510(k) (2 devices).
What risk classes do Inter-Os Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inter-Os Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inter-Os Technologies in the registry?
The most recently registered devices listed for Inter-Os Technologies include INTER-OS BONE GENERATOR and INTER-OS LIMB LENGTHENER.