Sicage, LLC is one of 20110 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Sicage, LLC has 1 FDA 510(k) cleared medical devices. Based in Souix Falls, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sicage, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sicage, LLC
1 devices