G-Floss & G-Floss II

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K911701 ↗

FDA Product Code

JES

Device Class

Class I

Regulation

21 CFR Part 872.6390

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Abutment Glo

  Class I

  FDA 510(k) K905303 Active Cleared 10 Jun 1991

• Implant Innovation Pre-Angled Abutment System

  Class II

  FDA 510(k) K932123 Active Cleared 27 May 1994

• Abutment Head Post

  Class II

  FDA 510(k) K871954 Active Cleared 31 Jul 1987

• Adbutment Cylinder and Screw

  Class II

  FDA 510(k) K871863 Active Cleared 10 Jul 1987

• Post. Screw & Hex Driver/Adbut & Adbut Head Driver

  Class II

  FDA 510(k) K871862 Active Cleared 10 Jul 1987

• 3I Standard Threaded/Self-Tapping Threaded Implants Modification

  Class II

  FDA 510(k) K935544 Active Cleared 13 Mar 1995

See all devices from Implant Innovations International, Inc. →