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Denture, Restoration Surgical guide

FDA UDI

Class N (US FDA UDI)

by Aceso Dental Laboratory Company Limited

Identity

Trade Name
Denture, Restoration Surgical guide FDA UDI
Generic Name
Complete upper denture FDA UDI
Model / Reference
998 FDA UDI

Identifiers

Primary DI / UDI-DI
08936214229987 FDA UDI
FDA Product Code
NSO FDA UDI
NSP FDA UDI
NSL FDA UDI
NSJ FDA UDI
NSN FDA UDI
NDP FDA UDI
NSQ FDA UDI
NSK FDA UDI
GMDN Term
Complete upper denture FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
872.3980 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 dentureCustom-made orthopaedic/craniofacial surgical guideDental bridge, polymerDental casting non-noble alloy

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

Similar devices

Also classified as Custom-made dental crown, metal/polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 162c7869-5252-4d19-b1cb-b6e411e807f6 32 fields · synced May 30, 2026