Malaytex USA, Inc.
Country not established
- Devices
- 1
What Malaytex USA, Inc. makes
Malaytex USA, Inc. manufactures hypoallergenic latex exam gloves infused with cranberry extract, designed for medical examinations and procedures.
The company’s portfolio is regulated under FDA’s Class I device classification and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Malaytex USA, Inc. have in the registry?
The registry currently lists 1 device for Malaytex USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Malaytex USA, Inc.'s devices?
Among its 1 most recently registered device, Malaytex USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Malaytex USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Malaytex USA, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Malaytex USA, Inc. in the registry?
The most recently registered devices listed for Malaytex USA, Inc. include HYPOALLERGENIC CRANBERRY/MALAYTEX LATEX EXAM GLOVE.