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ZZ BASE DI-IL-WMSM-L12 Pilastro E.M. 3.75 (White Metal Scanmarker L12 ZBED11634L12

by Zirkonzahn GmbH

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 NumberD800ZBED11634L12 UDI-DI Date27 Sep 2021ListedStatusListed 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  • Withdrawn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
ZZ BASE DI-IL-WMSM-L12 Pilastro E.M. 3.75 (White Metal Scanmarker L12
Generic Name
Dental implant suprastructure, temporary, preformed, reusable
Model / Reference
ZBED11634L12
Description
Compatible with DentalTech ImpLassic _ Implogic White Metal Scanmarker consisting of: 1x White Metal Scanmarker L12 1x White Metal Scanmarker Screw
Primary DI / UDI-DI
D800ZBED11634L12
FDA Product Code
NDP
GMDN Term
Dental implant suprastructure, temporary, preformed, reusable
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Dental implant suprastructure, temporary, preformed, reusable

Other devices from Zirkonzahn GmbH

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Properties

  • Implantable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No