LIMIS Development B.V. is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
LIMIS Development B.V. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
LIMIS Development B.V. has 1 FDA 510(k) cleared medical devices. Based in Leeuwarden, NL.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by LIMIS Development B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - LIMIS Development B.V.
1 devices