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Yucera D2

by Shenzhen Yurucheng Dental Materials Co., Ltd. 26 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06942445559870 UDI-DI Date13 Oct 2025ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Yucera
Generic Name
Dental appliance fabrication material, ceramic
Model / Ref / Catalog
D2, ST U-shape(89×71×25)mm
Primary DI / UDI-DI
06942445559870
510(k) Number
FDA Product Code
PKJ
GMDN Term
Dental appliance fabrication material, ceramic
Device Class
N
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

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Other devices from Shenzhen Yurucheng Dental Materials Co., Ltd.

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Properties

  • Single Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No