Eidolon Corp.
Country not established
- Devices
- 1
What Eidolon Corp. makes
Eidolon Corp. manufactures the Eidolon Endoscope Coupler, a device designed to connect and adapt endoscope components for compatibility and ease of use in medical imaging procedures.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The product is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Eidolon Endoscope Coupler Ref K942141
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eidolon Corp. have in the registry?
The registry currently lists 1 device for Eidolon Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eidolon Corp.'s devices?
Among its 1 most recently registered device, Eidolon Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Eidolon Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eidolon Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eidolon Corp. in the registry?
The most recently registered devices listed for Eidolon Corp. include EIDOLON ENDOSCOPE COUPLER.