Sterisil
United Statesfrom the FDA registration address FDA FEI 3005844469
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Sterisil Antimicrobial Tubing And Bottle Ref K031681
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3005844469
- Address
- 4220 Mark Dabling Blvd, Colorado Spgs, CO, 80907
Frequently asked questions
How many devices does Sterisil have in the registry?
The registry currently lists 1 device for Sterisil. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterisil's devices?
Among its 1 most recently registered device, Sterisil has devices listed in FDA 510(k) (1 device).
What risk classes do Sterisil's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterisil's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sterisil in the registry?
The most recently registered devices listed for Sterisil include STERISIL ANTIMICROBIAL TUBING AND BOTTLE.