Lacerta Life Sciences is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lacerta Life Sciences - FDA 510(k) Cleared Devices
Recent clearances: LacertaMatrix
1
Total
1
Cleared
0
Denied
Lacerta Life Sciences has 1 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Latest FDA clearance: Feb 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lacerta Life Sciences Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Lacerta Life Sciences
1 devices