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DTX PMMA 98x20mm CLR 117476

by Argen Corporation, the

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD818117476 UDI-DI Date14 Mar 2022ListedStatusListed 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  • Withdrawn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
DTX PMMA 98x20mm CLR
Generic Name
Dental acrylic resin
Model / Ref / Catalog
117476
Primary DI / UDI-DI
D818117476
FDA Product Code
EBG
GMDN Term
Dental acrylic resin
Device Class
Class II
Regulation Number
872.3770
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental acrylic resin

Other devices from The Argen Corporation

See all devices from The Argen Corporation →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No