Hayes Medical, Inc.

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Web: http://www.hayesmed.com
E-Mail:
Address: 1115 Windfield Way, Ste. 100, El Dorado Hills, California 95762-9623, USA
Phone: +1-(916)-355-7100 | Fax: +1-(916)-355-7190 | Map/Directions >>
 
 

Profile: Hayes Medical, Inc. concentrates on the orthopaedic implant and instrument industry. Our Consensus® hip system offers the surgeon a variety of implant options, thus providing excellent performance for a wide spectrum of patient indications. Our UniSyn® hip system allows independent adjustment of both the size and orientation of each component.Our Consensus®Hip system offers the surgeon a variety of implant options, providing performance for a wide spectrum of patients.

The company was founded in 1992, has revenues of USD 5-10 Million, has ~50 employees and is ISO 9001, CE certified.

FDA Registration Number: 2952369

1 to 50 of 54 Products/Services (Click for related suppliers)  Page: [1] 2 >> Next 50 Results
• AC-Powered Motor Orthopedic Surgical Instrument (FDA Code: HWE / 878.4820)
Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.
• Antibiotic Medicated Bandages
• Broach (FDA Code: HTQ / 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.
• Calicum-Phosphate Non-Porous Metal/Polymer Uncemented Semi-Constrained Hip Prosthesis (FDA Code: MEH / 888.3353)
A hip joint metal/ceramic/polymer semi-constrained cemented or nonporous uncemented prosthesis is a device intended to be implanted to replace a hip joint. This device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. The two-part femoral component consists of a femoral stem made of alloys to be fixed in the intramedullary canal of the femur by impaction with or without use of bone cement. The proximal end of the femoral stem is tapered with a surface that ensures positive locking with the spherical ceramic (aluminium oxide, A1203) head of the femoral component. The acetabular component is made of ultra-high molecular weight polyethylene or ultra-high molecular weight polyethylene reinforced with nonporous metal alloys, and used with or without bone cement.
• Calipers (FDA Code: KTZ / 888.4150)
A caliper for clinical use is a compass-like device intended for use in measuring the thickness or diameter of a part of the body or the distance between two body surfaces, such as for measuring an excised skeletal specimen to determine the proper replacement size of a prosthesis.
• Cemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: JDI / 888.3350)
A hip joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and an acetabular resurfacing component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027).
• Compression Garments
• Depth Gauge (FDA Code: HTJ / 888.4300)
A depth gauge for clinical use is a measuring device intended for various medical purposes, such as to determine the proper length of screws for fastening the ends of a fractured bone.
• Drill Bit (FDA Code: HTW / 888.4540)
• Engineering/Design Service
• Equipment Contract Research & Development
• Flexible Depth Gauge (FDA Code: HTJ / 888.4300)
• General Medical Supplies
• Hip Positioner Systems
• Hip Products
• Impactor (FDA Code: HWA / 888.4540)
• Knee Products
• Knee Systems
• Knee/Ankle Braces & Supports
• Lateral Tibial Inserts
• Lymphedema Compression Garments
• Medial Tibial inserts
• Medicated Bandages
• Metal/Polymer Femoral Hemi- Hip Prosthesis (FDA Code: KWY / 888.3390)
A hip joint femoral (hemi-hip) metal/polymer cemented or uncemented prosthesis is a two-part device intended to be implanted to replace the head and neck of the femur. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a snap-fit acetabular component made of an alloy, such as cobalt-chromium-molybdenum, and ultra-high molecular weight polyethylene. This generic type of device may be fixed to the bone with bone cement (888.3027) or implanted by impaction.
• Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LPH / 888.3358)
A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.
• Modular Hip System
• Nail Extractors (FDA Code: HWB / 888.4540)
• Non-Powered Traction Apparatus (FDA Code: HST / 888.5850)
A nonpowered orthopedic traction apparatus is a device that consists of a rigid frame with nonpowered traction accessories, such as cords, pulleys, or weights, and that is intended to apply a therapeutic pulling force to the skeletal system.
• Orthopedic Implant Devices
• Orthopedic instruments, total knee Systems
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Orthopedic Surgical Dc-Powered Motor and Accessory/Attachment (FDA Code: KIJ / 878.4820)
• Patellar Implants
• Pneumatic Powered Orthopedic Surgical Instrument & Accessory (FDA Code: HSZ / 878.4820)
• Polyethylene Tibial Inserts
• Post-Surgery Compression Garments
• Quality Control Equipment/Service
• Reamer (FDA Code: HTO / 888.4540)
• Reconstructive Total Joint Implants for Hip
• Reconstructive Total Joint Implants for Knee
• Screwdriver (FDA Code: HXX / 888.4540)
• Semi-Constrained Acetabular Hip Prosthesis (FDA Code: KWA / 888.3330)
A hip joint metal/metal semi-constrained, with an uncemented acetabular component, prosthesis is a two-part device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that consist of a femoral and an acetabular component, both made of alloys, such as cobalt-chromium-molybdenum. The femoral component is intended to be fixed with bone cement. The acetabular component is intended for use without bone cement (888.3027).
• Semi-Constrained Hip Prosthesis (FDA Code: JDL / 888.3320)
A hip joint metal/metal semi-constrained, with a cemented acetabular component, prosthesis is a two-part device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that consist of a femoral and an acetabular component, both made of alloys, such as cobalt-chromium-molybdenum. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).
• Semi-Constrained Patellofemorotibial Knee Prosthesis (FDA Code: JWH / 888.3560)
A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).
• Small Depth Gauge (FDA Code: HTJ / 888.4300)
• Stabilized Total Knee Systems
• Templates (FDA Code: HWT / 888.4800)
A template for clinical use is a device that consists of a pattern or guide intended for medical purposes, such as selecting or positioning orthopedic implants or guiding the marking of tissue before cutting.
• Tibial Inserts
• Total Knee Prosthesis
• Total Knee Systems

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