Ryoden Intl., Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Ryoden Intl., Ltd. makes
Ryoden Intl., Ltd. manufactures latex patient examination gloves designed for clinical use, ensuring barrier protection during medical procedures.
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 Gloves (Latex) Ref K892300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ryoden Intl., Ltd. have in the registry?
The registry currently lists 1 device for Ryoden Intl., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ryoden Intl., Ltd.'s devices?
Among its 1 most recently registered device, Ryoden Intl., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ryoden Intl., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ryoden Intl., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ryoden Intl., Ltd. in the registry?
The most recently registered devices listed for Ryoden Intl., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).