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Anti-snoring, restoration

FDA UDI

Class II (US FDA UDI)

by Modern Dental Laboratory (DG) Co., Ltd.

Identity

Trade Name
Anti-snoring, restoration FDA UDI
Generic Name
Mandible-repositioning sleep-disordered breathing orthosis FDA UDI
Model / Reference
154 FDA UDI

Identifiers

Primary DI / UDI-DI
06972677871549 FDA UDI
FDA Product Code
LRK FDA UDI
NSP 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Custom-made dental crown, ceramicDental bridge, ceramicDental veneer, professionalMandible-repositioning sleep-disordered breathing orthosis

Anti-snoring, restoration by Modern Dental Laboratory (DG) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ceramic dental inlay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Modern Dental Laboratory (DG) Co., Ltd.

Sources (1)

  • FDA UDI 10d64a45-98d7-45c2-8032-a5e00dbff1e3 32 fields · synced Jun 8, 2026