Oratec Corp.
United Statesfrom the FDA registration address FDA FEI 1122110
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Syrette Ref K881992
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1122110
- Address
- 12181 Brady Lane, MANASSAS, VA, 20109
Frequently asked questions
How many devices does Oratec Corp. have in the registry?
The registry currently lists 1 device for Oratec Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oratec Corp.'s devices?
Among its 1 most recently registered device, Oratec Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Oratec Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oratec Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Oratec Corp. in the registry?
The most recently registered devices listed for Oratec Corp. include SYRETTE.