Ansell Edmont Industrial, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ansell Edmont Industrial, Inc. makes
The company manufactures powder-free nitrile medical examination gloves designed for single-use in clinical and healthcare settings, intended to reduce allergic reactions and provide tactile sensitivity for procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ansell Edmont Industrial, Inc. have in the registry?
The registry currently lists 2 devices for Ansell Edmont Industrial, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ansell Edmont Industrial, Inc.'s devices?
Among its 2 most recently registered devices, Ansell Edmont Industrial, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ansell Edmont Industrial, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ansell Edmont Industrial, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ansell Edmont Industrial, Inc. in the registry?
The most recently registered devices listed for Ansell Edmont Industrial, Inc. include NITRA-TOUCH POWDER-FREE NITRILE MEDICAL EXAMINATION GLOVE.