Interpore Hex Head Implant Restorative Components

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K912734 ↗

FDA Product Code

DZE

Device Class

Class II

Regulation

21 CFR Part 872.3640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Ultracon Ultrafiltrator

  Class II

  FDA 510(k) K981253 Active Cleared 11 Dec 1998

• Imz Membrane Tack System

  Class II

  FDA 510(k) K960945 Active Cleared 24 May 1996

• Interpore Ip 200 Granular Coralline Hydroxyapatite Bone Void Fillers, 425 to 1000 Microns and 425 to 600 Microns

  Class II

  FDA 510(k) K950165 Active Cleared 28 Mar 1995

• Imz Intramobile Cylinder Implant

  Class II

  FDA 510(k) K855032 Active Cleared 3 Mar 1986

• Interpore Cylindrical Hex Implant, 3.3 Mm Diameter

  Class II

  FDA 510(k) K922732 Active Cleared 10 Feb 1994

• Interpore 200 Porous Hydroxyapatite

  Class II

  FDA 510(k) K860983 Active Cleared 23 May 1986

See all devices from Interpore Intl. →