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ZQuiet S.A.

FDA UDI

Class II (US FDA UDI)

by Sleeping Well, LLC

Identity

Trade Name
ZQuiet S.A. FDA UDI
Generic Name
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI
Device Name
ZQuiet S.A. Dental Size A Single Unit FDA UDI
Model / Reference
ZQSA-XDA FDA UDI
Description
ZQuiet S.A. Dental Size A Single Unit FDA UDI

Identifiers

Primary DI / UDI-DI
00858522003234 FDA UDI
510(k) Number
K140777 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mandible-repositioning sleep-disordered breathing orthosis

ZQuiet S.A. by Sleeping Well, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K140777 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sleeping Well, LLC

Sources (1)

  • FDA UDI 3507bcd9-c68d-49f2-bfc0-9df20098c51b 34 fields · synced Jun 8, 2026