C.E.I.B.Med
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What C.E.I.B.Med makes
C.E.I.B.Med manufactures the Reon, a medical device designed for specific diagnostic or therapeutic applications within its Class II category. The product appears to be a single device focused on a targeted clinical use, though exact details are not provided.
The Reon is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Reon Ref K250763
510(k) 510(k)
Frequently asked questions
How many devices does C.E.I.B.Med have in the registry?
The registry currently lists 1 device for C.E.I.B.Med. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.E.I.B.Med's devices?
Among its 1 most recently registered device, C.E.I.B.Med has devices listed in FDA 510(k) (1 device).
What risk classes do C.E.I.B.Med's devices fall under?
Among its 1 most recently registered device, the classes recorded for C.E.I.B.Med's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C.E.I.B.Med in the registry?
The most recently registered devices listed for C.E.I.B.Med include Reon.