Kensey Nash Corporation

Address: 735 Pennsylvania Drive, Exton, Pennsylvania 19341, USA
Phone: +1-(484)-713-2100 | Fax: +1-(484)-713-2900 | Map/Directions >>

Profile: Kensey Nash Corporation is a medical device company that deals with the development of a wide variety of products for the cardiovascular, endovascular, sports medicine, spine and trauma marketplaces. We have developed and commercialized a series of novel endovascular devices in the market segments of thrombus management and chronic total occlusions (CTO). We deal with endovascular products and biomaterials. We manufacture both proprietary and OEM biomaterial components for customers who incorporate them into their own products. Our current biomaterials development programs encompass products for soft tissue repair, spine and trauma, orthobiologics and drug/device combinations. Our Angio-Seal™ vascular closure device consists of three resorbable components namely an anchor, a collagen sponge and a suture along with a delivery system that closes the puncture. The anchor & suture act as a pulley to position the collagen into the puncture tract adjacent to the outside of the artery wall to seal and close the puncture & effect hemostasis. Our OsseoFit™ porous tissue matrix ™ (PTM) device is intended to be gently packed into bone voids or bone defects in the pelvis and extremities. It utilizes several resorbable biomaterials including a proprietary collagen formulation, synthetic polymer and ceramic. Its unique design provides a stable platform for cell in-growth that will ultimately be replaced completely by bone during the healing process.

The company was founded in 1984, has revenues of USD 50-100 Million, has ~360 employees and is ISO 9001, CE certified. NASDAQ:KNSY (SEC Filings)

FDA Registration Number: 2530154

30 Products/Services (Click for related suppliers)  
• Bone Fixation Plate (FDA Code: HRS / 888.3030)
Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
• Bone Fixation Screw (FDA Code: HWC / 888.3040)
A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.
• Bone Trephine (FDA Code: HWK / 888.4540)
An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.
• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)
A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.
• Dental Bioresorbable Barrier Matrix
• Dental Surgical Dressing Material
• Distal Embolic Protection Devices
• Drill Bit (FDA Code: HTW / 888.4540)
• Embolic Protection System
• Equipment Contract Research & Development
• Extraction Catheter
• Guide Catheter, Embolic Protection
• Hemostatic Puncture Closure Device
• Medical Probes (FDA Code: HXB / 888.4540)
• Membrane Prosthesis
• Metal Mesh (FDA Code: EZX / 878.3300)
Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Orthopedic Tray Set (FDA Code: OJH / 878.4800)
A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.
• Peripheral Transluminal Angioplasty Catheter (FDA Code: LIT / 870.1250)
A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.
• Platelet Aggregation and Adhesion Collagen
• Probes (FDA Code: HXB / 888.4540)
• Probes (FDA Code: HXB / 888.4540)
• Product Design & Development
• Resorbable Beta-tricalcium Phosphate
• Soft Tissue Biodegradable Fixation Fastener (FDA Code: MAI / 888.3030)
• Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060)
A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.
• Surgical Mesh (FDA Code: FTM / 878.3300)
• Synthetic Polymer
• Tamps (FDA Code: HXG / 888.4540)
• Vascular Closure Device

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