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Denture

FDA UDI

Class N (US FDA UDI)

by Aceso Dental Laboratory Company Limited

Identity

Trade Name
Denture FDA UDI
Generic Name
Complete upper denture FDA UDI
Device Name
Full dentures are manufactured as finished products from denture resins. FDA UDI
Model / Reference
003 FDA UDI
Description
Full dentures are manufactured as finished products from denture resins. FDA UDI

Identifiers

Primary DI / UDI-DI
08936214220038 FDA UDI
FDA Product Code
NSL FDA UDI
GMDN Term
Complete upper 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: Complete upper dentureComplete lower denture

Denture by Aceso Dental Laboratory Company Limited — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Complete lower denture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 631fd7ff-23e5-41c6-9beb-df540451ed4b 33 fields · synced May 31, 2026