Seamark Technologies
Country not established
- Devices
- 1
What Seamark Technologies makes
Seamark Technologies manufactures the Dolomite Rollator, a mobility aid designed to assist individuals with limited mobility in walking and transferring while providing support and stability.
The Dolomite Rollator is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dolomite Rollator Ref K921917
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seamark Technologies have in the registry?
The registry currently lists 1 device for Seamark Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seamark Technologies's devices?
Among its 1 most recently registered device, Seamark Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Seamark Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Seamark Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seamark Technologies in the registry?
The most recently registered devices listed for Seamark Technologies include DOLOMITE ROLLATOR.