Teratech Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teratech Corporation - FDA 510(k) Cleared Devices
Recent clearances: Terason uSmart 3200T Plus Ultrasound System, Terason uSmart3200T Ultrasound System
2
Total
2
Cleared
0
Denied
Teratech Corporation has 2 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Teratech Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Teratech Corporation
2 devices