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Denture, Restoration 302

by Aceso Dental Laboratory Company Limited

Denture, Restoration 302 is a device classified as Not classified made by Aceso Dental Laboratory Company Limited, listed in FDA GUDID since 17 Oct 2022 (UDI-DI 08936214223022), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08936214223022 UDI-DI Date17 Oct 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Denture, Restoration
Generic name
Dental casting noble alloy
Model / reference
302
Primary DI / UDI-DI
08936214223022
FDA product code
NSJ, NSL, NSP
GMDN term
Dental casting noble alloy
Device class
N
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Custom-made dental crown, ceramicDental bridge, ceramicDental casting noble alloyDental veneer, professional

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)