Manufacturer registered with FDA

The Snore Reliever Company

Largo, FL, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.

FDA owner/operator10033460Repacker / relabelerSpecification developer

Device types listed: 1
Brands and models: 1
510(k) clearances: 22010–2021
Markets registered in: 1United States
Establishments: 1United States

510(k) clearances per year, 2007–2026

Devices listed with FDA

What The Snore Reliever Company currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Anti-Snoring DeviceLRK · Class 2	Anti-snoring & jaw-repositioning devices	Maker	Vital Sleep	2010

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names The Snore Reliever Company as the applicant.

Decided	510(k)	Device	Device type
14 Jan 2021	K201719	Vital Sleep	LRK Anti-Snoring Device
13 Jan 2010	K092942	VITAL SLEEP	LRK Anti-Snoring Device

Registered establishments

Establishment	Location	What it does
THE SNORE RELIEVER COMPANYFDA reg. 3008583502	Largo, FL, United States	Repacker / relabeler, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10033460). 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.