Dimedikorea
South KoreaFDA 510(k) applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Dimedikorea makes
Dimedikorea manufactures the Goyo Mouthpiece S, a device designed for oral hygiene or respiratory support applications, intended for use in medical or dental settings.
The Goyo Mouthpiece S is classified as a Class II (U) device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Goyo Mouthpiece S Ref K232238
510(k) 510(k)
FDA establishments
- Dimedi Korea Inc Busan · KR FEI 3029913483
Frequently asked questions
How many devices does Dimedikorea have in the registry?
The registry currently lists 1 device for Dimedikorea. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dimedikorea's devices?
Among its 1 most recently registered device, Dimedikorea has devices listed in FDA 510(k) (1 device).
What are the newest devices from Dimedikorea in the registry?
The most recently registered devices listed for Dimedikorea include Goyo Mouthpiece S.
Which FDA establishments are linked to Dimedikorea?
1 FDA establishment is linked to Dimedikorea in the registry; they are listed on the company page.