Implantology Module, Model 2175

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K932492 ↗

FDA Product Code

JEY

Device Class

Class II

Regulation

21 CFR Part 872.4760

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Micro-Aire Soft-Ice, Cold Therapy Compress

  Class I

  FDA 510(k) K905207 Active Cleared 22 Jan 1991

• Fixation Devices and Bone Plate

  Class II

  FDA 510(k) K910175 Active Cleared 21 Jun 1991

• Micro-Aire Model 2060

  Class I

  FDA 510(k) K913369 Active Cleared 1 Nov 1991

• 2710-000 Oscillating Saw, General Assembly

  Class I

  FDA 510(k) K905383 Active Cleared 18 Jun 1991

• Microaire(R) Facial Bone Plating System

  Class II

  FDA 510(k) K914998 Active Cleared 2 Jun 1992

• Series 5000 Battery Powered Instrument System

  Class I

  FDA 510(k) K931395 Active Cleared 28 Jan 1994

See all devices from Micro Surgical Instruments Corp. →