Imodex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Imodex, Inc. makes
Imodex, Inc. makes the STATFLO and Carotid Balloon Shunt medical devices.
These devices are classified as Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Statflo Ref K880180
Regimes: 510(k) Registry: 510(k)Carotid Balloon Shunt Ref K860497
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Imodex, Inc. have in the registry?
The registry currently lists 2 devices for Imodex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Imodex, Inc.'s devices?
Among its 2 most recently registered devices, Imodex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Imodex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Imodex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Imodex, Inc. in the registry?
The most recently registered devices listed for Imodex, Inc. include STATFLO and CAROTID BALLOON SHUNT.