Skip to content

Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 5 Black 209005

by Clinician's Choice Dental Products, Inc.

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 Number07540172016544 UDI-DI Date19 Mar 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  • Withdrawn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
Dual-Force™ Sectional Matrix System Active-Wedge Refill Size 5 Black
Generic Name
Dental matrix band, single-use
Model / Ref / Catalog
209005
Primary DI / UDI-DI
07540172016544
FDA Product Code
DZN
GMDN Term
Dental matrix band, single-use
Device Class
Class I
Regulation Number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental matrix band, single-use

Other devices from Clinician's Choice Dental Products, Inc.

See all devices from Clinician's Choice Dental Products, Inc. →

Properties

  • Premarket Exempt

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: 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