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Good Morning Snore Solution

FDA UDI

Class II (US FDA UDI)

by Mpowrx Health and Wellness Products 2012, Inc.

Identity

Trade Name
Good Morning Snore Solution FDA UDI
Generic Name
Tongue-retaining sleep-disordered breathing orthosis FDA UDI
Device Name
The Good Morning Snore Solution - An intraoral device for the reduction of snoring for adults at least 18 years old. FDA UDI
Model / Reference
1 FDA UDI
Description
The Good Morning Snore Solution - An intraoral device for the reduction of snoring for adults at least 18 years old. FDA UDI

Identifiers

Primary DI / UDI-DI
00627843257127 FDA UDI
510(k) Number
K193239 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Tongue-retaining sleep-disordered breathing orthosis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tongue-retaining sleep-disordered breathing orthosis

Good Morning Snore Solution by Mpowrx Health and Wellness Products 2012, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tongue-retaining sleep-disordered breathing orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mpowrx Health and Wellness Products 2012, Inc.

Sources (1)

  • FDA UDI d2f10636-3f54-402b-8df8-34cbb59a5352 35 fields · synced May 30, 2026