Safeskin Corp.
United StatesFDA applicant, unverified
- Devices
- 24
What Safeskin Corp. makes
Safeskin Corp. manufactures patient examination gloves, including latex and nitrile varieties, both powdered and powder-free. Their portfolio includes hypoallergenic and sterile surgical gloves, as well as modified examination gloves and those designed for use with chemotherapeutic agents. The company also produces sterile purple nitrile examination gloves and hypoallergenic sterile examination gloves.
These devices are classified under Class I by the FDA and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Search and filter all 24 devicesFrequently asked questions
How many devices does Safeskin Corp. have in the registry?
The registry currently lists 24 devices for Safeskin Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safeskin Corp.'s devices?
Among its 24 most recently registered devices, Safeskin Corp. has devices listed in FDA 510(k) (24 devices).
What risk classes do Safeskin Corp.'s devices fall under?
Among its 24 most recently registered devices, the classes recorded for Safeskin Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Safeskin Corp. in the registry?
The most recently registered devices listed for Safeskin Corp. include NITRILE RUBBER EXAMINATION GLOVES (POWERED), NITRILE RUBBER POWDER-FREE EXAMINATION GLOVE, PATIENT EXAMINATION GLOVES (LATEX) and SAFESKIN PFE-XTRA POWDER-FREE LATEX EXAMINATION GLOVES, PROTEIN CONTENT 50 MCG OR LESS, FOR USE WITH CHEMOTHERAPEUTIC AG.