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Walser® matrices 031

by Dr. Walser Dental GmbH

Walser® matrices 031 is a Class I device made by Dr. Walser Dental GmbH, listed in FDA GUDID since 5 Dec 2022 (UDI-DI 04262363910709), 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 Number04262363910709 UDI-DI Date5 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  • Withdrawn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
Walser® matrices
Generic name
Rubber dam clamp forceps
Model / reference
031
Primary DI / UDI-DI
04262363910709
FDA product code
DZN
GMDN term
Rubber dam clamp forceps
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Instrument tray, reusableDental matrix band, reusableRubber dam clamp forceps

Similar devices in this category

Other devices filed under Rubber dam clamp forceps.

Other devices from Dr. Walser Dental GmbH

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Properties

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