Transtimulation Research, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Transtimulation Research, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.
Latest FDA clearance: Apr 2025. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Transtimulation Research, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by AlvaMed, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
2 devices