Osteomed Corp

Address: 3885 Arapaho Road, Addison, Texas 75001, USA
Phone: +1-(972)-677-4600 | Fax: +1-(972)-677-4601 | Map/Directions >>

Profile: Osteomed Corp is a global manufacturer and marketer of specialty medical devices, surgical implants and powered surgical instruments. We provide the surgeon with innovative products and state of the art rigid fixation systems. We offer products like craniomaxillofacial, distraction osteogenesis, small bone orthopedic, neurosurgical, osteobiologics & osteomatchTM. Our unique modular delivery systems and patented self-drilling screw technology represent the pinnacle of clinical technology. Our Mincro™ fixation system for onlay bone grafting and guided tissue regeneration procedures is an ideal office kit. Our OsteoDriver™ disposable autodriver eliminates the need for autoclaving and repairs.

The company was founded in 2002, has revenues of USD 25-50 Million, has ~180 employees and is ISO certified.

FDA Registration Number: 2027754

1 to 50 of 59 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.
• Bender (FDA Code: HXW / 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.
• Bio-Actionr Great Toe System
• BioresorbableT Fixation System
• Bone Clamp (FDA Code: HXD / 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.
• 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 Graft Regeneration Fixation Kit
• Bone Grafting Wheel
• Bone Plates, Calcaneal
• Bone Rasps (FDA Code: HTR / 878.4800)
• Bone Taps (FDA Code: HWX / 888.4540)
• Bone Void Filler
• Cannulated Screw Fracture Fixation System
• Cannulated Screw System
• Countersink (FDA Code: HWW / 888.4540)
• Cranial Clamp System
• 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)
• Flexible Depth Gauge (FDA Code: HTJ / 888.4300)
• Flexible Stabilization Rods
• Foot Fragment Sets
• Foot Implants Foot Fragment Sets
• Foot Implants, Mini Lag Screw Systems
• Forceps (FDA Code: HTD / 878.4800)
• Formable Craniofacial Mesh
• General & Plastic Saw Surgical Blade (FDA Code: GFA / 878.4820)
• General & Plastic Surgery Surgical Burr (FDA Code: GFF / 878.4820)
• General Surgical Manual Instrument (FDA Code: MDM / 878.4800)
• Hammertoe Implants
• Human Bone Rasps (FDA Code: HTR / 878.4800)
• Locking Fracture System
• Mandibular Distraction System
• Medical Rasps (FDA Code: HTR / 878.4800)
• Mid-Face Distraction System
• Mini Lag Screw Systems
• MP Joint Implants
• Neuro Fixation System
• Non-Alterable Preformed Skull Bone Plate (FDA Code: GXN / 882.5330)
A preformed nonalterable cranioplasty plate is a device that is implanted in a patient to repair a skull defect and is constructed of a material, e.g., stainless steel or vitallium, that cannot be altered or reshaped at the time of surgery without changing the chemical behavior of the material.
• Orthodontic Anchor System
• OrthognathicT System
• Orthopedic Surgical Dc-Powered Motor and Accessory/Attachment (FDA Code: KIJ / 878.4820)
• Orthopedics Foot Implants, MP Joint Implants
• Phalangeal Hemi- Toe Prosthesis (FDA Code: KWD / 888.3730)
A toe joint phalangeal (hemi-toe) polymer prosthesis is a device made of silicone elastomer intended to be implanted to replace the base of the proximal phalanx of the toe.
• Plastic Surgery Kit and Accessories (FDA Code: FTN / 878.3925)
A plastic surgery kit and accessories is a device intended to be used to reconstruct maxillofacial deficiencies. The kit contains surgical instruments and materials used to make maxillofacial impressions before molding an external prosthesis.
• Polymer Constrained Toe Prosthesis (FDA Code: KWH / 888.3720)
A toe joint polymer constrained prosthesis is a device made of silicone elastomer or polyester reinforced silicone elastomer intended to be implanted to replace the first metatarsophalangeal (big toe) joint. This generic type of device consists of a single flexible across-the-joint component that prevents dislocation in more than one anatomic plane.
• Reconstruction Locking System
• Screwdriver (FDA Code: HXX / 888.4540)
• Self-Drilling Screws
• Semi-Constrained Metal/Polymer Toe (Metatarsophalangeal) Joint Prosthesis (FDA Code: LZJ)

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