Joylux, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Joylux, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Joylux, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Joylux, Inc.
1 devices