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Overdenture Attachment

by Implant Innovations International, Inc.

510(k) K891613

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

6 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK891613 Date10 Oct 1989ClearedStatusActive

Recalls

6 recalls · FDA

  • 6 recalls, same reason

    • Terminated Z-2459-2016 FDA Class II initiated 25 Nov 2015
    • Terminated Z-2424-2016 FDA Class II initiated 25 Nov 2015
    • Terminated Z-2461-2016 FDA Class II initiated 25 Nov 2015
    • Terminated Z-2425-2016 FDA Class II initiated 25 Nov 2015
    • Terminated Z-2460-2016 FDA Class II initiated 25 Nov 2015
    • Terminated Z-2426-2016 FDA Class II initiated 25 Nov 2015

    Pouches may not have been sealed during packing.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DZE
Device Class
Class II
Regulation
21 CFR Part 872.3640
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

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