Teslake, Inc.
United Statesfrom the FDA registration address FDA FEI 3016496998
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Spinal System Ref K240963
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016496998
- Address
- 17150 Via Del Campo, San Diego, CA, 92127
Frequently asked questions
How many devices does Teslake, Inc. have in the registry?
The registry currently lists 1 device for Teslake, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teslake, Inc.'s devices?
Among its 1 most recently registered device, Teslake, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Teslake, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Teslake, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teslake, Inc. in the registry?
The most recently registered devices listed for Teslake, Inc. include Spinal System.