Dental Implants OKTAGON Tissue Level and Bone Level

No FDA recalls on record, checked 7 Oct 2026.

510(k) Number

K162073 ↗

FDA Product Code

DZE

Device Class

Class II

Regulation

21 CFR Part 872.3640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Meisinger Tacs (Meisinger Meitac-Kit), Meisinger Pins (Meisinger Master-Pin-Control-Kit, Basic-Kit

  Class II

  FDA 510(k) K130682 Active Cleared 13 Aug 2013

• Dental Implants OKTAGON Bone Level Tapered Design

  Class II

  FDA 510(k) K170287 Active Cleared 24 May 2017

• Dental Implant System

  Class II

  FDA 510(k) K122807 Active Cleared 13 Jun 2014

• Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)

  Class II

  FDA 510(k) K250123 Active Cleared 29 Sep 2025

• Abutment Rp, Abutment Wp, Burn-Out Coping, Screws, Titanium Adhesive Base, Alligator Abutment, Solid Abutment, Retentive

  Class II

  FDA 510(k) K132214 Active Cleared 7 Jul 2014

• Dental Implant OKTAGON Bone Level

  Class II

  FDA 510(k) K143539 Active Cleared 31 Aug 2015

See all devices from Hager& Meisinger GmbH →