Skip to the page

Data / Medical devices / Canada / MPOWRX HEALTH AND WELLNESS PRODUCTS 2012 Inc.

MPOWRX HEALTH AND WELLNESS PRODUCTS 2012 Inc.: FDA-registered device maker in Calgary Alberta, Canada, 1 510(k) clearance

MPOWRX HEALTH AND WELLNESS PRODUCTS 2012 Inc. is registered with the FDA (registration 3007616887) in Calgary Alberta, Canada. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated January 3, 2020. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3007616887
Address
16 Ave NW, Calgary Alberta, Canada, T2M 0K3
Owner or operator
MPowRx Health and Wellness Products 2012 Inc. (10028248)
Roles
Complaint file establishment, Specification developer
First device listed
January 7, 2020
Registered through
2026
Brand names listed
Good Morning Snore Solution, MPowRx Snoring Solution

Devices it lists

DeviceProduct codeClassRoleSource
Device, Anti-SnoringLRK2Complaint file establishment, Specification developeraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 3, 2020K193239MPowRx Snoring Solution (also known as Good Morning Snore Solution)LRKSubstantially EquivalentMpowrx Health and Wellness Products 2012, Inc.accessdata.fda.gov

Compare with other makers

Updated January 3, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.