Lazurite Holdings, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lazurite Holdings, LLC has 1 FDA 510(k) cleared medical devices. Based in Cleveland, US.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lazurite Holdings, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Lazurite Holdings, LLC
1 devices