Prosthetics & Instrumentation a. Prosthetic Abutments 4, 5, 6 Diameter, Grade 3, B. Irrigation Drills, Tooling & Preang'

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K953237 ↗

FDA Product Code

DZE

Device Class

Class II

Regulation

21 CFR Part 872.3640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Kis MT5

  Class II

  FDA 510(k) K960112 Active Cleared 15 Mar 1996

• Kis-V Pre-Angulated and Wide Body Abutments

  Class II

  FDA 510(k) K950893 Active Cleared 5 May 1995

• Abutment - Complete

  Class II

  FDA 510(k) K974280 Active Cleared 20 Feb 1998

• Screw Implants, Grade 3; Uncoated, Ha, Tp-B3

  Class II

  FDA 510(k) K953234 Active Cleared 8 Nov 1995

• Kis II Lg Hex Screw & Cylinder Implants

  Class II

  FDA 510(k) K953558 Active Cleared 19 Dec 1995

• Kis MT3

  Class II

  FDA 510(k) K960110 Active Cleared 20 Mar 1996

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