Lapis Lazuli International NV is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lapis Lazuli International NV - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lapis Lazuli International NV has 1 FDA 510(k) cleared medical devices. Based in Grand Junction,, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Lapis Lazuli International NV Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lapis Lazuli International NV
1 devices