Dental Device Guide
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Not currently registered with FDA under this name

Sleepwright

Santa Fe, NM, United States. Named as applicant on 1 dental 510(k) clearance between 2011 and 2011. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12011–2011
Markets registered in
1United States
Establishments
0—
2011: 120102020

510(k) clearances per year, 2007–2026

510(k) clearances

Clearances on which FDA names Sleepwright as the applicant.

Decided510(k)DeviceDevice type
12 May 2011K101155AURADORM (NEUROMUSCULAR SLEEP)LRK Anti-Snoring Device

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.