Siats, LLC is one of 20092 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siats, LLC - FDA 510(k) Cleared Devices
Recent clearances: T-Rex Standalone ALIF
1
Total
1
Cleared
0
Denied
Siats, LLC has 1 FDA 510(k) cleared medical devices. Based in Tulsa, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Siats, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Siats, LLC
1 devices