Geenli Plastic Co, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Geenli Plastic Co, Ltd. makes
Geenli Plastic Co, Ltd. manufactures powder-free vinyl patient examination gloves in clear, non-colored form. These gloves are designed for single-use medical examinations and procedures, providing a barrier between healthcare providers and patients.
The company’s vinyl gloves fall under FDA Class I regulatory classification and are listed via the 510(k) pathway in the United States. The products are intended for use within the scope of their designated classification and comply with applicable U.S. regulatory requirements.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Geenli Plastic Co, Ltd. have in the registry?
The registry currently lists 1 device for Geenli Plastic Co, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geenli Plastic Co, Ltd.'s devices?
Among its 1 most recently registered device, Geenli Plastic Co, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Geenli Plastic Co, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Geenli Plastic Co, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Geenli Plastic Co, Ltd. in the registry?
The most recently registered devices listed for Geenli Plastic Co, Ltd. include POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED).