Biopsy Forceps

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K892252 ↗

FDA Product Code

FCL

Device Class

Class I

Regulation

21 CFR Part 876.1075

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Scissors: Thorek, Jorgensen, Finochietto

  Class I

  FDA 510(k) K891203 Active Cleared 6 Apr 1989

• Zeppelin Scissors

  Class I

  FDA 510(k) K891049 Active Cleared 17 Mar 1989

• Rectal Specula - Chelsea-Eaton, Kelly, Mathieu

  Class I

  FDA 510(k) K892542 Active Cleared 9 May 1989

• Zsi Biopsy Forceps

  Class I

  FDA 510(k) K891027 Active Cleared 17 Mar 1989

• Dental Root Elevator

  Class II

  FDA 510(k) K892255 Active Cleared 1 May 1989

• Vaginal Retractors - Kristeller, Delee, Breisky

  Class I

  FDA 510(k) K891038 Active Cleared 17 Mar 1989

See all devices from Zinnanti Surgical Instruments, Inc. →