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