Troutman Corneal Punch

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K771866 ↗

FDA Product Code

HRH

Device Class

Class I

Regulation

21 CFR Part 886.4350

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Farrior Oval Speculum

  Class I

  FDA 510(k) K772380 Active Cleared 17 Jan 1978

• Endoscopic Needlholder Cat. Number 114705

  Class II

  FDA 510(k) K911272 Active Cleared 2 Jul 1991

• Hooks #'s 7600, 7602, 7603, 7616

  Class I

  FDA 510(k) K791985 Active Cleared 4 Oct 1979

• Neivs Tracheotomy Retractor

  Class I

  FDA 510(k) K772378 Active Cleared 9 Mar 1978

• Hemoclip X-20 Automatic Hemoclip Ligating Applier

  Class II

  FDA 510(k) K844836 Active Cleared 23 Jan 1985

• Weck Tying Forcep, Straight Titanium

  Class I

  FDA 510(k) K761251 Active Cleared 16 Dec 1976

See all devices from Edward Weck, Inc. →