Institut Georges Lopez is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Institut Georges Lopez - FDA 510(k) Cleared Devices
Recent clearances: PERF-GEN Pulsatile Perfusion Solution, BEL-GEN Cold Storage Solution, RM4 Control Unit
3
Total
3
Cleared
0
Denied
Institut Georges Lopez has 3 FDA 510(k) cleared medical devices. Based in Lissieu, FR.
Last cleared in 2022. Active since 2021. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Institut Georges Lopez Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Institut Georges Lopez
3 devices