OMNI life science, Inc.

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Web: http://www.omnils.com
E-Mail:
Address: 175 Paramount dr., Raynham, Massachusetts 02767, USA
Phone: +1-(508)-824-2444 | Fax: +1-(508)-822-6030 | Map/Directions >>
 
 

Profile: Omni Life Science designs, produces and distributes orthotic devices. We specialize in knee bracing and measurement systems. We offer products like hip & knee reconstruction. Our Apex Modular™ femoral stem system is designed to provide surgeons with a concise and logical set of options to accurately restore joint mechanics, leg length discrepancy & soft tissue balance. Our Apex K2 modular has a dual taper stem combined with modular necks and heads that allows surgeons to precisely address patient specific anatomical needs to achieve accurate leg length & soft tissue balance.

The company was founded in 1998, has revenues of USD 1-5 Million, has ~40 employees and is ISO 13485 ,CE Certification, MDSS Certification certified.

FDA Registration Number: 2918697

1 to 50 of 69 Products/Services (Click for related suppliers)  Page: [1] 2 >> Next 50 Results
• Acetabular Cup System
• Adjustable Ankle Support
• Air Ankle Support
• Ankle Support
• Anterior Closure Hinged Knee Support
• Basic Ankle Support
• Basic Knee Support
• 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.
• Closed Patella Knee Support
• 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.
• Double Stay Knee Support
• Double Stay Visco Knee Support
• Double-Strap Ankle Support
• Drill Bit (FDA Code: HTW / 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.
• Elastic Ankle Support
• Elastic Cartilage Knee Support
• Elastic Hinged Knee Support
• Elastic Knee Support
• Elastic Shoulder Immobilizer
• Elastic Spiral Knee Support
• Excelerator Stirrup-Style Ankle Support
• External Brace Knee Joint (FDA Code: ITQ / 890.3475)
A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement. Examples of limb orthoses include the following: A whole limb and joint brace, a hand splint, an elastic stocking, a knee cage, and a corrective shoe.
• Femoral Stem Systems
• Flexible Depth Gauge (FDA Code: HTJ / 888.4300)
• Foot Support
• Foot Support Positioning System
• Gel Ankle Support
• Hip Replacement, Femoral Heads
• Humeral Splints
• Instrument Surgical Guide (FDA Code: FZX / 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.
• Knee Support
• Knee Support Pillow
• Leather Lacing Ankle Support
• Limb Brace Orthosis (FDA Code: IQI / 890.3475)
• Lower Extremity Splints
• Magnetic Knee Support
• Medical Devices
• 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.
• Neoprene Ankle Support
• Neoprene Hinged Knee Support with Straps
• Neoprene Knee Support with Sping
• Neoprene Open Knee Support
• Opend Patella Knee Support
• Orthopaedic Reconstruction
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Orthopedic Reconstruction Products
• Orthoses, Humeral Splints
• Orthosis
• Patella Tracking Stabilizer Knee Supports
• Patellofemoral Replacement Systems

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