Geon Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
Catalogue
Geon Digital Clinical Thermometer Ref K003223
510(k) 510(k)- GUDID
Geon Electronic Thermometer Ref K952001
510(k) 510(k)
Frequently asked questions
How many devices does Geon Corp. have in the registry?
The registry currently lists 3 devices for Geon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geon Corp.'s devices?
Among its 3 most recently registered devices, Geon Corp. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Geon Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Geon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Geon Corp. in the registry?
The most recently registered devices listed for Geon Corp. include GEON DIGITAL CLINICAL THERMOMETER, Geon MT-B162A and GEON ELECTRONIC THERMOMETER.