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Restoration 352

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

Restoration 352 is a device classified as Not classified made by Modern Dental Laboratory (DG) Co., Ltd., listed in FDA GUDID since 24 Jul 2020 (UDI-DI 06972677873529), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06972677873529 UDI-DI Date24 Jul 2020ListedStatusListed 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  • Withdrawn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
Restoration
Generic name
Dental casting noble alloy
Model / reference
352
Primary DI / UDI-DI
06972677873529
FDA product code
NSJ, NSP, NSQ
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: Dental casting non-noble alloyCustom-made dental crown, ceramicDental bridge, ceramicDental casting noble alloy

Other devices from Modern Dental Laboratory (DG) Co., Ltd.

See all devices from Modern Dental Laboratory (DG) Co., Ltd. →

Properties

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