Seeram Products Development
Country not established
- Devices
- 1
What Seeram Products Development makes
Seeram Products Development manufactures the SEERAM BLADE, a surgical cutting instrument designed for precision tissue dissection.
The SEERAM BLADE is classified under FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Seeram Blade Ref K844073
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seeram Products Development have in the registry?
The registry currently lists 1 device for Seeram Products Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seeram Products Development's devices?
Among its 1 most recently registered device, Seeram Products Development has devices listed in FDA 510(k) (1 device).
What are the newest devices from Seeram Products Development in the registry?
The most recently registered devices listed for Seeram Products Development include SEERAM BLADE.