Manufacturer registered with FDA

MPowRx Health and Wellness Products 2012 Inc.

Calgary, Canada. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10028248Specification developer

Device types listed: 1
Brands and models: 2
510(k) clearances: 12020–2020
Markets registered in: 1United States
Establishments: 1Canada

510(k) clearances per year, 2007–2026

Devices listed with FDA

What MPowRx Health and Wellness Products 2012 Inc. 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	Good Morning Snore SolutionMPowRx Snoring Solution	2020

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 MPowRx Health and Wellness Products 2012 Inc. as the applicant.

Decided	510(k)	Device	Device type
3 Jan 2020	K193239	MPowRx Snoring Solution (also known as Good Morning Snore Solution)	LRK Anti-Snoring Device

Registered establishments

Establishment	Location	What it does
MPOWRX HEALTH AND WELLNESS PRODUCTS 2012 Inc.FDA reg. 3007616887	Calgary Alberta, Canada	Complaint file establishment, Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10028248). 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.