The Snore Reliever Company, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
The Snore Reliever Company, LLC has 2 FDA 510(k) cleared medical devices. Based in Laguna Niguel, US.
Last cleared in 2021. Active since 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by The Snore Reliever Company, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Devine Guidance International, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - The Snore Reliever Company, LLC
2 devices