Plymouth, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Plymouth, Ltd. makes
Plymouth, Ltd. manufactures latex patient examination gloves.
The company is based in the US and its products are listed in the FDA 510k registry as Class I devices.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Latex Patient Examination Glove Ref K895497
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Plymouth, Ltd. have in the registry?
The registry currently lists 1 device for Plymouth, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Plymouth, Ltd.'s devices?
Among its 1 most recently registered device, Plymouth, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Plymouth, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Plymouth, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Plymouth, Ltd. in the registry?
The most recently registered devices listed for Plymouth, Ltd. include LATEX PATIENT EXAMINATION GLOVE.