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Jiahong dental lab JH-PRE-EKO-001

by Shenzhen Jiahong Dental Technology Co., Ltd.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06979878380047 UDI-DI Date3 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Jiahong dental lab
Generic Name
Preformed complete denture
Model / Reference
JH-PRE-EKO-001
Primary DI / UDI-DI
06979878380047
FDA Product Code
EKO
GMDN Term
Preformed complete denture
Device Class
Class II
Regulation Number
872.3600
GUDID distribution status
In Commercial Distribution

Other devices from Shenzhen Jiahong Dental Technology Co., Ltd.

Properties

  • Manufacturing Date

Other properties (13)

  • Sterile: No
  • Single Use: 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
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No