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Henry Schein® Eugenol, USP 1710504FG

by Dentsply International

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD6871710504FG2 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Henry Schein® Eugenol, USP
Generic Name
Denture reliner, soft, professional
Model / Ref / Catalog
1710504FG
Primary DI / UDI-DI
D6871710504FG2
FDA Product Code
EMB
GMDN Term
Denture reliner, soft, professional
Device Class
Class I
Regulation Number
872.3275
GUDID distribution status
Not in Commercial Distribution
Size
Total Volume — 4 Fluid Ounce

Other devices from Dentsply International

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Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • 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
  • Serial Number: No
  • Manufacturing Date: No