Bonn Micro Iris Hook (Non-Sterile) #7613

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

510(k) Number

K801469 ↗

FDA Product Code

HNQ

Device Class

Class I

Regulation

21 CFR Part 886.4350

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

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  Class I

  FDA 510(k) K772380 Active Cleared 17 Jan 1978

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  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

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  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. →