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Hook, Ophthalmic

FDA product code HNQ · Class 1 · Ophthalmic

3,932
Registered devices
109
Adverse events
4
Recalls
10
510(k) clearances

Devices with this code

23ga Morris ILM Pick, Carbon Fiber Handle — KATALYST SURGICAL LLCWalcott Rx Products — Walcott Rx Product IncWalcott Rx Products — Walcott Rx Product IncIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMR PHACO — Crestpoint Management LimitedAESCULAP — AESCULAP, INC.MR PHACO — Crestpoint Management LimitedDuckworth & Kent — DUCKWORTH AND KENT LIMITEDMSI Precision Specialty Instruments — Med Saver, Inc.Ambler Surgical — AMBLER SURGICAL CORP.Ambler Surgical — AMBLER SURGICAL CORP.Millennium — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.Ambler Surgical — AMBLER SURGICAL CORP.MSI Precision Specialty Instruments — Med Saver, Inc.Walcott Rx Products — Walcott Rx Product IncMR PHACO — Crestpoint Management LimitedOph.Hook — KATENA PRODUCTS, INC.Diamatrix Ltd. — DiamatrixIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONMORIA — MORIA SAWalcott Rx Products — Walcott Rx Product IncV. Mueller — CAREFUSION 2200, INCSurgical Goniotomy Lens, Ring/Handle — KATALYST SURGICAL LLC

Recent recalls

DateFirmReason
2025-12-16Vortex Surgical Inc.There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of biob
2025-12-16Vortex Surgical Inc.There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of biob
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2022-03-16Carl Zeiss Meditec AGHigh friction of the slider can cause the device to stick, or not move as intended.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.