Moss Point Glove Co.
Country not established
- Devices
- 1
What Moss Point Glove Co. makes
Moss Point Glove Co. manufactures the N-DEX, a nitrile examination glove designed for medical and clinical use. These gloves are intended to provide barrier protection during procedures requiring dexterity and sensitivity, such as patient examinations or minor surgical tasks.
The N-DEX falls under FDA Class I regulatory classification and is listed via the 510(k) pathway. The company operates within the United States, adhering to domestic regulatory requirements for medical devices.
Catalogue
N-Dex Ref K902696
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Moss Point Glove Co. have in the registry?
The registry currently lists 1 device for Moss Point Glove Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Moss Point Glove Co.'s devices?
Among its 1 most recently registered device, Moss Point Glove Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Moss Point Glove Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Moss Point Glove Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Moss Point Glove Co. in the registry?
The most recently registered devices listed for Moss Point Glove Co. include N-DEX.