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MOLEKUR Express Foil-0.375-300

by Shanghai Coherz 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 Number06975527186138 UDI-DI Date30 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  • Withdrawn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
Molekur
Generic Name
Dental appliance fabrication material, thermoplastic
Model / Reference
Express Foil-0.375-300
Primary DI / UDI-DI
06975527186138
FDA Product Code
EBH, DYJ
GMDN Term
Dental appliance fabrication material, thermoplastic
Device Class
Class I
Regulation Number
872.3670, 872.5410
GUDID distribution status
In Commercial Distribution

Other devices from Shanghai Coherz Technology Co., Ltd.

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Properties

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

Other properties (8)

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