Novalis Medical, LLC is one of 23657 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novalis Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: CLAREON AND SOLARUS PULSED LIGHT DEVICES AND ACCESSORIES
1
Total
1
Cleared
0
Denied
Novalis Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Novalis Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Novalis Medical, LLC
1 devices