The Snore Reliever Company, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Snore Reliever Company, LLC - FDA 510(k) Cleared Devices
Recent clearances: Vital Sleep
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