Mediplus (India) Limited is one of 87 FDA 510(k) medical device manufacturers from India in the dataset, ranked by real submission volume.
Mediplus (India) Limited - FDA 510(k) Cleared Devices
Recent clearances: Pluski Safe 1 Safety IV Catheter
1
Total
1
Cleared
0
Denied
Mediplus (India) Limited has 1 FDA 510(k) cleared medical devices. Based in Bahadurgarh, IN.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mediplus (India) Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mediplus (India) Limited
1 devices