Yon'S Jay Enterprise Co.
TaiwanFDA applicant, unverified
- Devices
- 3
What Yon'S Jay Enterprise Co. makes
Yon'S Jay Enterprise Co. manufactures Class I medical devices, including the product listed under its own name, which appears to be a non-generic device.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices classified as Class I. The company is based in the United States.
Catalogue
Sunglasses Ref K941668
Regimes: 510(k) Registry: 510(k)Yon's Jay Enterprise Co Ref K940730
Regimes: 510(k) Registry: 510(k)None-Generic Ref K940725
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Yon'S Jay Enterprise Co. have in the registry?
The registry currently lists 3 devices for Yon'S Jay Enterprise Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yon'S Jay Enterprise Co.'s devices?
Among its 3 most recently registered devices, Yon'S Jay Enterprise Co. has devices listed in FDA 510(k) (3 devices).
What risk classes do Yon'S Jay Enterprise Co.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Yon'S Jay Enterprise Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Yon'S Jay Enterprise Co. in the registry?
The most recently registered devices listed for Yon'S Jay Enterprise Co. include SUNGLASSES, YON'S JAY ENTERPRISE CO and NONE-GENERIC.