Freiler
Country not established
- Devices
- 1
What Freiler makes
Freiler manufactures the OCTOSTIM, a device designed for cardiac pacing and rhythm management, used in implantable neurostimulation applications.
The OCTOSTIM 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
Octostim Ref K951682
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Freiler have in the registry?
The registry currently lists 1 device for Freiler. Devices recorded under merged duplicate company entries are counted once.
Which registries list Freiler's devices?
Among its 1 most recently registered device, Freiler has devices listed in FDA 510(k) (1 device).
What risk classes do Freiler's devices fall under?
Among its 1 most recently registered device, the classes recorded for Freiler's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Freiler in the registry?
The most recently registered devices listed for Freiler include OCTOSTIM.