Seemac Reison Ab Co.
SwedenFDA applicant, unverified
- Devices
- 1
What Seemac Reison Ab Co. makes
Seemac Reison AB Co. manufactures the SWEMAC REISON BIPLANAR 300, which is a Class II medical device.
The company is based in the US and its device is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Swemac Reison Biplanar 300 Ref K911739
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seemac Reison AB Co. have in the registry?
The registry currently lists 1 device for Seemac Reison AB Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seemac Reison AB Co.'s devices?
Among its 1 most recently registered device, Seemac Reison AB Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Seemac Reison AB Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Seemac Reison AB Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seemac Reison AB Co. in the registry?
The most recently registered devices listed for Seemac Reison AB Co. include SWEMAC REISON BIPLANAR 300.