Polyviolene Suture-Revised Labeling

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K926167 ↗

FDA Product Code

GAT

Device Class

Class II

Regulation

21 CFR Part 878.5000

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Look Irrigating/Aspirating Cannula W/Teflon Sheath

  Class I

  FDA 510(k) K872884 Active Cleared 10 Aug 1987

• Look Irrigating Cystotomes

  Class I

  FDA 510(k) K870439 Active Cleared 20 Feb 1987

• Look Viscodissector

  Class II

  FDA 510(k) K913530 Active Cleared 21 Oct 1991

• Sterile Black Monofilament Nylon Non-Absor. Suture

  Class II

  FDA 510(k) K903029 Active Cleared 25 Oct 1990

• Ophthalmic PAO Valve

  Class II

  FDA 510(k) K882536 Active Cleared 9 Sep 1988

• Look Retrobulbar Needles

  Class I

  FDA 510(k) K870902 Active Cleared 20 Mar 1987

See all devices from Look, Inc. →