Regent Group Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Regent Group Co., Ltd. makes
Regent Group Co., Ltd. manufactures latex examination gloves, designed for medical and clinical use to ensure barrier protection during patient examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Examination Gloves Ref K893263
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Regent Group Co., Ltd. have in the registry?
The registry currently lists 1 device for Regent Group Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Regent Group Co., Ltd.'s devices?
Among its 1 most recently registered device, Regent Group Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Regent Group Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Regent Group Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Regent Group Co., Ltd. in the registry?
The most recently registered devices listed for Regent Group Co., Ltd. include LATEX EXAMINATION GLOVES.