Vibe 2000
Country not established
- Devices
- 1
What Vibe 2000 makes
Vibe 2000 manufactures the JEJE Teether, a pacifier-style oral device designed for infant oral health and teething relief.
The JEJE Teether is classified as a Class I medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Jeje Teether Ref K034017
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vibe 2000 have in the registry?
The registry currently lists 1 device for Vibe 2000. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vibe 2000's devices?
Among its 1 most recently registered device, Vibe 2000 has devices listed in FDA 510(k) (1 device).
What risk classes do Vibe 2000's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vibe 2000's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vibe 2000 in the registry?
The most recently registered devices listed for Vibe 2000 include JEJE TEETHER.