Vibe 2000 is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vibe 2000 - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Vibe 2000 has 1 FDA 510(k) cleared medical devices. Based in Lake Forest, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Vibe 2000 Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vibe 2000
1 devices