Lelo, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Lelo, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Mar 2025. Active since 2016. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Lelo, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Insight, Inc. as regulatory consultant.
3 devices