Sterigard, Inc.
Country not established
- Devices
- 1
What Sterigard, Inc. makes
Sterigard, Inc. manufactures hypoallergenic latex patient examination gloves.
These Class I medical devices are based in the US and are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Latex Patient Examination Gloves, Hypoallergenic Ref K912083
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sterigard, Inc. have in the registry?
The registry currently lists 1 device for Sterigard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterigard, Inc.'s devices?
Among its 1 most recently registered device, Sterigard, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sterigard, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterigard, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sterigard, Inc. in the registry?
The most recently registered devices listed for Sterigard, Inc. include LATEX PATIENT EXAMINATION GLOVES, HYPOALLERGENIC.