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Gutta Percha Points Feathered Tip Mf

by DiaDent Group International 9 variants

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 Number08806383509060 UDI-DI Date7 Apr 2020ListedStatusListed 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  • Withdrawn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
Gutta Percha Points
Generic Name
Natural gutta-percha
Model / Ref / Catalog
FEATHERED TIP MF, 156-573
Primary DI / UDI-DI
08806383509060
FDA Product Code
EKM
GMDN Term
Natural gutta-percha
Device Class
Class I
Regulation Number
872.3850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Natural gutta-percha

Other devices from DiaDent Group International

See all devices from DiaDent Group International →

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt

Other properties (11)

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