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Clamp, Penile

FDA product code FHA · Class 1 · Gastroenterology, Urology

49

Registered devices

26

Adverse events

1

Recalls

11

510(k) clearances

Devices with this code

Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft MSI Precision Specialty Instruments — Med Saver, Inc.Novo Surgical — NOVO SURGICAL, INC.RZ Medizintechnik GmbH — RZ-Medizintechnik GmbH Jeato Incontinence Clamp — Jeato Med. CO., Ltd.MSI Precision Specialty Instruments — Med Saver, Inc.Incontinence Clamp — C. R. Bard, Inc.Symmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.KindKlamp — ARGENTUM MEDICAL, LLC Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.Penile Clamp — C. R. Bard, Inc.V. Mueller — STERIS CORPORATION Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.Jeato 7 Incontinence Clamp — Jeato Med. CO., Ltd.KindKlamp — ARGENTUM MEDICAL, LLC Greenwald Surgical Company, Inc. — GRACE MANUFACTURING, INC.KindKlamp — ARGENTUM MEDICAL, LLC V. Mueller — STERIS CORPORATION Ambler Surgical — AMBLER SURGICAL CORP.MSI Precision Specialty Instruments — Med Saver, Inc.Incontinence Clamp — C. R. Bard, Inc.

Recent recalls

Date	Firm	Reason
2018-02-16	Aesculap Implant Systems LLC	The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable.

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