Siloam, Inc.
Country not established
- Devices
- 1
What Siloam, Inc. makes
Siloam, Inc. makes the Siloam Save-A-Needle device.
The device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Siloam Save-A-Needle Ref K820502
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siloam, Inc. have in the registry?
The registry currently lists 1 device for Siloam, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siloam, Inc.'s devices?
Among its 1 most recently registered device, Siloam, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Siloam, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Siloam, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Siloam, Inc. in the registry?
The most recently registered devices listed for Siloam, Inc. include SILOAM SAVE-A-NEEDLE.