Libent Co., Ltd.
Country not established
- Devices
- 2
What Libent Co., Ltd. makes
Libent Co., Ltd. manufactures patient examination gloves, including standard vinyl and powder-free vinyl varieties, designed for clinical use.
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
Patient Examination Gloves (Vinyl) Ref K891945
Regimes: 510(k) Registry: 510(k)Powder Free Vinyl Examination Gloves Ref K893883
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Libent Co., Ltd. have in the registry?
The registry currently lists 2 devices for Libent Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Libent Co., Ltd.'s devices?
Among its 2 most recently registered devices, Libent Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Libent Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Libent Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Libent Co., Ltd. in the registry?
The most recently registered devices listed for Libent Co., Ltd. include PATIENT EXAMINATION GLOVES (VINYL) and POWDER FREE VINYL EXAMINATION GLOVES.