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Denture, splint

FDA UDI

Class N (US FDA UDI)

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

Identity

Trade Name
Denture, splint FDA UDI
Generic Name
Complete lower denture FDA UDI
Model / Reference
112 FDA UDI

Identifiers

Primary DI / UDI-DI
06972677871129 FDA UDI
FDA Product Code
NSL FDA UDI
NSR FDA UDI
GMDN Term
Complete lower denture FDA UDI

Classification

Device Class
N 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

Yes

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: Orthodontic retainerComplete upper dentureComplete lower dentureRemovable dental occlusal splint, preformed

Denture, splint by Modern Dental Laboratory (DG) Co., Ltd. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Removable dental occlusal splint, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4e6a596e-5095-4b7a-b3ec-4d947477f98e 32 fields · synced May 30, 2026