Mds
Country not established
- Devices
- 1
What Mds makes
Mds manufactures the Bi-Directional Spiral & Epoxy Root Canal Cement System, a dental material designed for root canal treatments to seal and fill the root canal space.
This product is classified as a Class II medical device in the US and is listed under FDA 510(k) clearance. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mds have in the registry?
The registry currently lists 1 device for Mds. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mds's devices?
Among its 1 most recently registered device, Mds has devices listed in FDA 510(k) (1 device).
What risk classes do Mds's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mds's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mds in the registry?
The most recently registered devices listed for Mds include THE BI-DIRECTIONAL SPIRAL & EPOXY ROOT CANAL CEMENT SYSTEM.