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Denture

FDA UDI

Class N (US FDA UDI)

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

Identity

Trade Name
Denture FDA UDI
Generic Name
Partial denture FDA UDI
Device Name
Partial dentures are manufactured as finished products from denture resins and other supporting materials. FDA UDI
Model / Reference
012 FDA UDI
Description
Partial dentures are manufactured as finished products from denture resins and other supporting materials. FDA UDI

Identifiers

Primary DI / UDI-DI
06972677870122 FDA UDI
FDA Product Code
NSK FDA UDI
GMDN Term
Partial 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: Partial denture

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

Similar devices

Also classified as Partial denture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af234640-ab35-439f-ad6d-0da2eae3c4c8 33 fields · synced May 30, 2026