JVCKENWOOD Corporation
Active in EUDAMEDJapanfrom SRN EUDAMED FDA SRN JP-MF-000023544 FEI 1000207387
- Devices
- 43
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
- Authorised rep.
- JVCKENWOOD Deutschland GmbHDE
Catalogue
Search and filter all 43 devicesCompany details
- EUDAMED SRN
- JP-MF-000023544
- FDA FEI number
- 1000207387
- EUDAMED status
- Active
- EUDAMED registered name
- JVCKENWOOD Corporation
- EUDAMED abbreviated name
- JVCKENWOOD
- Registered address
- 3-12, Moriya-cho, 221-0022, Yokohama-shi, Kanagawa, Japan
- Website
- www.jvckenwood.com/en.html
- [email protected]
- PRRC contact
- Takayuki Kasahara
Frequently asked questions
How many devices does JVCKENWOOD Corporation have in the registry?
The registry currently lists 43 devices for JVCKENWOOD Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list JVCKENWOOD Corporation's devices?
Among its 43 most recently registered devices, JVCKENWOOD Corporation has devices listed in EUDAMED (21 devices) and FDA 510(k) (22 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do JVCKENWOOD Corporation's devices fall under?
Among its 43 most recently registered devices, the classes recorded for JVCKENWOOD Corporation's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from JVCKENWOOD Corporation in the registry?
The most recently registered devices listed for JVCKENWOOD Corporation include CL-S200BF0EA, CL-S600BN0EA, CL-R211BN0EA and CL-E270WA0EA.