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SnoreMD

FDA UDI

Class II (US FDA UDI)

by Apnea Sciences Corporation

Identity

Trade Name
SnoreMD FDA UDI
Generic Name
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI
Device Name
Mouth Guard FDA UDI
Model / Reference
1 FDA UDI
Description
Mouth Guard FDA UDI

Identifiers

Primary DI / UDI-DI
00861481000305 FDA UDI
510(k) Number
K112205 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Mandible-repositioning 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

Yes

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mandible-repositioning sleep-disordered breathing orthosis

SnoreMD by Apnea Sciences Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mandible-repositioning sleep-disordered breathing orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apnea Sciences Corporation

Sources (1)

  • FDA UDI 4365e609-2d1a-4f65-a9f9-802fdd8f079d 34 fields · synced May 30, 2026