Trans1
Also registered as Trans1, Inc.
United Statesfrom the FDA registration address FDA FEI 3011302058
- Devices
- 5
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
TranS1 AxiaLIF Plus System Ref K192792
Regimes: 510(k) Registry: 510(k)TRANS1LATERAL Interbody Fusion System Ref K123997
Regimes: 510(k) Registry: 510(k)TRANS1 Axial Fixation System Ref K040426
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
TranS1 Interbody Fusion System Ref K191791
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3011302058
- Address
- 32938 Tamina Rd., Magnolia, TX, 77354
Frequently asked questions
How many devices does Trans1 have in the registry?
The registry currently lists 5 devices for Trans1. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trans1's devices?
Among its 5 most recently registered devices, Trans1 has devices listed in FDA 510(k) (5 devices).
What risk classes do Trans1's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Trans1's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trans1 in the registry?
The most recently registered devices listed for Trans1 include TranS1 AxiaLIF Plus System, TRANS1LATERAL INTERBODY FUSION SYSTEM, TRANS1 AXIAL FIXATION SYSTEM and TRANS1 TRANS-SACRAL SPINAL ACCESS AND PREPARATION KIT.