Rejuvena Ent. Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Rejuvena Ent. Co., Ltd. makes
Rejuvena Ent. Co., Ltd. manufactures patient examination gloves, which are designed for single-use clinical procedures to maintain hygiene and reduce infection risk during medical examinations.
These products fall under FDA Class I regulatory classification and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K890858
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rejuvena Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Rejuvena Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rejuvena Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Rejuvena Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Rejuvena Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rejuvena Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rejuvena Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Rejuvena Ent. Co., Ltd. include PATIENT EXAMINATION GLOVES.