Gtimd, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gtimd, LLC - FDA 510(k) Cleared Devices
Recent clearances: Aqueduct 200 Cervical Dilation Balloon Catheter, Aqueduct 100 Plus Cervical Dilation Balloon Catheter
3
Total
3
Cleared
0
Denied
Gtimd, LLC has 3 FDA 510(k) cleared medical devices. Based in Amherst, US.
Last cleared in 2021. Active since 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Gtimd, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gtimd, LLC
3 devices