Tenma Co., Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Tenma Co., Ltd. makes
Tenma Co., Ltd. manufactures patient examination gloves.
The company is based in the US, and its products are classified as Class I medical devices listed in the FDA 510(k) database.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves Ref K893618
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tenma Co., Ltd. have in the registry?
The registry currently lists 1 device for Tenma Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tenma Co., Ltd.'s devices?
Among its 1 most recently registered device, Tenma Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tenma Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tenma Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tenma Co., Ltd. in the registry?
The most recently registered devices listed for Tenma Co., Ltd. include PATIENT EXAMINATION GLOVES.