Forceps-Orthopedic

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K890165 ↗

FDA Product Code

LXN

Device Class

Class I

Regulation

21 CFR Part 870.4500

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Towel Clips

  Class I

  FDA 510(k) K890159 Active Cleared 3 Feb 1989

• Ronguer-Orthopedic

  Class I

  FDA 510(k) K890166 Active Cleared 13 Feb 1989

• Extractor for Austin Moore Femoral Head

  Class I

  FDA 510(k) K890162 Active Cleared 13 Feb 1989

• Gouges for Femoral Heads

  Class I

  FDA 510(k) K890160 Active Cleared 13 Feb 1989

• Retractors

  Class I

  FDA 510(k) K890158 Active Cleared 13 Feb 1989

• Holder, Needle

  Class I

  FDA 510(k) K890167 Active Cleared 3 Feb 1989

See all devices from Dhason Brothers, Inc. →