Si-Technology, LLC
United StatesFDA applicant, unverified FDA FEI 3012103114
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Si-Technology, LLC makes
Si-Technology, LLC manufactures sacroiliac joint fusion systems, including the SI-DESIS® X™ and SI-DESIS® screws, designed for spinal stabilization procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Si-Technology® Si-Desis® Screws Ref K151462
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3012103114
- Address
- 7842 Hickory Flat Hwy, Woodstock, GA, 30188
Frequently asked questions
How many devices does Si-Technology, LLC have in the registry?
The registry currently lists 3 devices for Si-Technology, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Si-Technology, LLC's devices?
Among its 3 most recently registered devices, Si-Technology, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Si-Technology, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Si-Technology, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Si-Technology, LLC in the registry?
The most recently registered devices listed for Si-Technology, LLC include SI-TECHNOLOGY® SI-DESIS® X™ Sacroiliac Joint Fusion System and SI-TECHNOLOGY® SI-DESIS® SCREWS.