Roundworks Technologies Private Limited is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Roundworks Technologies Private Limited - FDA 510(k) Cleared Devices
Recent clearances: Alveoair Digital Spirometer
1
Total
1
Cleared
0
Denied
Roundworks Technologies Private Limited has 1 FDA 510(k) cleared medical devices. Based in Wakad, Pune, IN.
Last cleared in 2023. Active since 2023. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Roundworks Technologies Private Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by IZiel Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - Roundworks Technologies Private Limited
1 devices