Lacerta Life Science - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Lacerta Life Science has 1 FDA 510(k) cleared medical devices. Based in Broussard, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lacerta Life Science Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
1 devices