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Kinetic Medical Products

Country not established

Devices
63

What Kinetic Medical Products makes

Kinetic Medical Products manufactures surgical instruments for obstetrics, gynecology, and general surgery, including clamps for intestinal and parametrial use, forceps for cervical biopsies and uterine dressings, a malleable placenta curette, rib shears, and a vaginal speculum.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue63

Newest first, rows 1-50 of 63

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  • Intestinal Crushing Clamp Ref K890371

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Septum Elevator Ref K890365

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Intestinal Clamp Ref K890372

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Cervical Biopsy Forceps Ref K890380

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Uterine Dressing Forceps Ref K890378

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Artery Forceps Ref K890246

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Vaginal Speculum Ref K890376

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Malleable Placenta Curette Ref K890387

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Parametrium Clamp Ref K890381

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Rib Shears Ref K890259

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Bone Curette Ref K890252

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Uterine Curette Ref K890384

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Hemorrhoidal Forceps Ref K890373

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Gall Stone Forceps Ref K890369

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Scalpel Handle Ref K890242

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Catheter Forceps Ref K890238

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Placenta And Ovum Forceps Ref K890386

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Surgical Needle Guide Ref K890228

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Kidney Clamp Ref K890368

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgical Elevator Ref K890253

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Dressing Scissors Ref K890235

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microsurgical Needle Holders Ref K890211

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Tubing Clamp Forceps Ref K890244

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgical Scissors Ref K890225

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Bone Shears Ref K890260

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microsurgical Scissors Ref K890212

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgical Probe Ref K890227

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Bone Rongeur, Double-Action Ref K890256

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Dressing Forceps Ref K890243

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Umbilical Scissors Ref K890389

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Cephalotomy Scissors Ref K890388

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Surgical Retractors Ref K890248

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Hysterectomy Forceps Ref K890383

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Adenoid Curette Ref K890366

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgical Forceps Ref K890226

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Bone Cutting Forceps, Double-Action Ref K890257

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microsurgical Forceps Ref K890213

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Ligature Needles Ref K890230

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Compression Forceps Ref K890382

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bone Cutting Forceps, Single-Action Ref K890258

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microsurgical Wire Loop Ref K890221

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Midwifery/Obstetrical Forceps Ref K890385

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bone Rongeur, Single-Action Ref K890255

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Suture Clip Applier/Remover Ref K890233

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Cilia Forceps Ref K890263

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Surgical Hemostats Ref K890245

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microsurgical Knives Ref K890217

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Abdominal Spatula Ref K890374

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Uterine Tentaculum Ref K890379

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Surgical Needle Holders Ref K890229

    Active Regimes: 510(k) Registry: 510(k) Class:I

Rows 1-50 of 63

Showing 1-50 of 63

Frequently asked questions

How many devices does Kinetic Medical Products have in the registry?

The registry currently lists 63 devices for Kinetic Medical Products. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kinetic Medical Products's devices?

Among its 50 most recently registered devices, Kinetic Medical Products has devices listed in FDA 510(k) (50 devices).

What risk classes do Kinetic Medical Products's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Kinetic Medical Products's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kinetic Medical Products in the registry?

The most recently registered devices listed for Kinetic Medical Products include INTESTINAL CRUSHING CLAMP, SEPTUM ELEVATOR, INTESTINAL CLAMP and CERVICAL BIOPSY FORCEPS.

Generated automatically from registry data and not verified by a human reviewer.