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Microdont 10.309.008

by 3R - Industria E Comercio Eireli

Microdont 10.309.008 is a Class I device made by 3R - Industria E Comercio Eireli, listed in FDA GUDID since 18 Jan 2022 (UDI-DI 07898229802955), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07898229802955 UDI-DI Date18 Jan 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Microdont
Generic name
Dental abrasive strip, single-use
Model / Ref / Catalog
10.309.008
Primary DI / UDI-DI
07898229802955
FDA product code
EHM
GMDN term
Dental abrasive strip, single-use
Device class
Class I
Regulation number
872.6010
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive strip, single-use

Similar devices

Other devices filed under FDA product code EHM (Strip, Polishing Agent).

Other devices from 3R - Industria E Comercio Eireli

See all devices from 3R - Industria E Comercio Eireli →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)