Lujena, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Lujena, Inc. has 2 FDA 510(k) cleared medical devices. Based in El Cajon, US.
Latest FDA clearance: May 2024. Active since 2023. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Lujena, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Matrix Medical Consulting, Inc. as regulatory consultant.
2 devices