Filliscope, Inc.
Country not established
- Devices
- 1
What Filliscope, Inc. makes
Filliscope, Inc. manufactures the FILLISCOPE, a device designed for endoscopic visualization and imaging of internal anatomical structures, primarily used in gastrointestinal procedures.
The FILLISCOPE is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Filliscope Ref K930804
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Filliscope, Inc. have in the registry?
The registry currently lists 1 device for Filliscope, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Filliscope, Inc.'s devices?
Among its 1 most recently registered device, Filliscope, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Filliscope, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Filliscope, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Filliscope, Inc. in the registry?
The most recently registered devices listed for Filliscope, Inc. include FILLISCOPE.