QuietLab, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
QuietLab, LLC has 1 FDA 510(k) cleared medical devices. Based in New York, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by QuietLab, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beanstock Consulting as regulatory consultant.
1 devices