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ContacEZ Restorative

by Directa AB 5 variants

ContacEZ Restorative (31009) is a Class I device made by Directa AB, listed in FDA GUDID since 6 Dec 2022 (UDI-DI 17310230310092), 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 Number17310230310092 UDI-DI Date6 Dec 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  • Withdrawn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
ContacEZ
Generic name
Dental abrasive strip, single-use
Model / Ref / Catalog
Restorative, 31009
Primary DI / UDI-DI
17310230310092
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

Related devices

Category: Dental abrasive strip, single-use

Other devices from Directa AB

See all devices from Directa AB →

Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)