Yaung Jenn Co., Ltd.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 1
What Yaung Jenn Co., Ltd. makes
Yaung Jenn Co., Ltd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Glove, Latex Ref K890971
510(k) 510(k)
Frequently asked questions
How many devices does Yaung Jenn Co., Ltd. have in the registry?
The registry currently lists 1 device for Yaung Jenn Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yaung Jenn Co., Ltd.'s devices?
Among its 1 most recently registered device, Yaung Jenn Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Yaung Jenn Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Yaung Jenn Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Yaung Jenn Co., Ltd. in the registry?
The most recently registered devices listed for Yaung Jenn Co., Ltd. include PATIENT EXAMINATION GLOVE, LATEX.