Boxspine, LLC
United Statesfrom the FDA registration address FDA establishment FEI 3027807601
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Duet™ Spinal Fixation System Ref K253169
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3027807601
- Address
- 3501 Miller Dr, Plymouth, IN, 46563
Frequently asked questions
How many devices does BOXSPINE, LLC have in the registry?
The registry currently lists 1 device for BOXSPINE, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list BOXSPINE, LLC's devices?
Among its 1 most recently registered device, BOXSPINE, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do BOXSPINE, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for BOXSPINE, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from BOXSPINE, LLC in the registry?
The most recently registered devices listed for BOXSPINE, LLC include Duet™ Spinal Fixation System.