3Dsharp, Inc.
Country not established
- Devices
- 1
What 3Dsharp, Inc. makes
3Dsharp, Inc. manufactures the 3DFIS, model IES-FL-101, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
3DFIS, Model Ies-Fl-101 Ref K013841
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does 3Dsharp, Inc. have in the registry?
The registry currently lists 1 device for 3Dsharp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list 3Dsharp, Inc.'s devices?
Among its 1 most recently registered device, 3Dsharp, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do 3Dsharp, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for 3Dsharp, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from 3Dsharp, Inc. in the registry?
The most recently registered devices listed for 3Dsharp, Inc. include 3DFIS, MODEL IES-FL-101.