Orient Commercial Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Orient Commercial Co., Ltd. makes
Orient Commercial Co., Ltd. manufactures latex patient examination gloves designed for clinical use, providing a barrier for medical professionals during procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Patient Examination Gloves Ref K894995
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orient Commercial Co., Ltd. have in the registry?
The registry currently lists 1 device for Orient Commercial Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orient Commercial Co., Ltd.'s devices?
Among its 1 most recently registered device, Orient Commercial Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Orient Commercial Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orient Commercial Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Orient Commercial Co., Ltd. in the registry?
The most recently registered devices listed for Orient Commercial Co., Ltd. include LATEX PATIENT EXAMINATION GLOVES.