Skip to content

Wirobond C

by Bego U.S.A. 510(k)

Active United States

510(k) K032136

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK032136 Date4 Sep 2003ClearedStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
EJH
Device Class
Class II
Regulation
21 CFR Part 872.3710
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

Other devices from Bego U.S.A.

  • Aurolloyd Kf

    Class II

  • Begopal

    Class II

  • Bio PontoStar

    Class II

  • Platinlloyd 100

    Class II

  • Begocer G

    Class II

  • Gold Dental Casting Alloys

    Class II