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SnoreByte Express

FDA UDI

Class II (US FDA UDI)

by Braebon Medical Corp.

Identity

Trade Name
SnoreByte Express FDA UDI
Generic Name
Mandible-repositioning/palate-lifting sleep-disordered breathing orthosis FDA UDI
Device Name
Kit including the Silent Sleep tray, intended as a temporary or trial device in the treatment of snoring or obstructive sleep apnea. Kit contains Silent Sleep Tray, bite wheel, carrying case. FDA UDI
Model / Reference
3530 FDA UDI
Description
Kit including the Silent Sleep tray, intended as a temporary or trial device in the treatment of snoring or obstructive sleep apnea. Kit contains Silent Sleep Tray, bite wheel, carrying case. FDA UDI

Identifiers

Catalog Number
3530 FDA UDI
Primary DI / UDI-DI
B14035301 FDA UDI
510(k) Number
K082849 FDA UDI
FDA Product Code
LRK FDA UDI
GMDN Term
Mandible-repositioning/palate-lifting 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

Yes

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

Yes

FDA UDI

Category: Mandible-repositioning/palate-lifting sleep-disordered breathing orthosis

SnoreByte Express by Braebon Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mandible-repositioning/palate-lifting sleep-disordered breathing orthosis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5b7bbdd9-3f5a-4a50-b433-e058a527e8e5 36 fields · synced May 30, 2026