Safetyfix Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Safetyfix Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SafetyFix EasyOut System
1
Total
1
Cleared
0
Denied
Safetyfix Medical Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Safetyfix Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Safetyfix Medical Technologies, Inc.
1 devices