Latexon Co., Ltd.
Country not established
- Devices
- 1
What Latexon Co., Ltd. makes
Latexon Co., Ltd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
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 K892622
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Latexon Co., Ltd. have in the registry?
The registry currently lists 1 device for Latexon Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Latexon Co., Ltd.'s devices?
Among its 1 most recently registered device, Latexon Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Latexon Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Latexon Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Latexon Co., Ltd. in the registry?
The most recently registered devices listed for Latexon Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).