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3I Patient-Specific Dental Abutment and Overdenture Bar

by Implant Innovations, Inc.

510(k) K032263

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 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 NumberK032263 Date28 Jan 2004ClearedStatusActive

Recalls

1 recall · FDA

    • Terminated Z-1215-2014 FDA Class II initiated 26 Aug 2013 on shared 510(k) K032263

    Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures were received.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

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  • Withdrawn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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