Profile: Biomet, Inc designs and manufactures products for hip replacement, knee replacement, shoulder replacement, elbow replacement & other small joint replacements. We are an ISO 9001 CE certified company. We offer products like joint replacement, sports medicine & dental implants. We encourage you to talk to your doctor about options that could help you get back to living and keep you active. If you have suffered from a sports related or other injury, we can help. Sports knee injuries and the available treatment options is the first step to making an informed decision about your healthcare and your quality of life. Our recommendation is to see an orthopedic physician who, after an examination, can give you the appropriate treatment options for your medical condition. Our Repicci II® implant system resurfaces only the damaged section of cartilage, thus saving a healthy cartilage. Our BioSymMetRic™ PIP fixator is a device that uses pins placed through the finger bone to stabilize complex finger fractures.

The company was founded in 1977, has revenues of > USD 1 Billion, has ~20 employees and is ISO 9001, CE certified. NASDAQ:BMET (SEC Filings)

FDA Registration Number: 1825034

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• Carpal Tunnel Release Kits

• Cartilage Repair Implants

• Cast Bandage (FDA Code: ITG / 890.3025) A prosthetic and orthotic accessory is a device intended for medical purposes to support, protect, or aid in the use of a cast, orthosis (brace), or prosthesis. Examples of prosthetic and orthotic accessories include the following: A pelvic support band and belt, a cast shoe, a cast bandage, a limb cover, a prosthesis alignment device, a postsurgical pylon, a transverse rotator, and a temporary training splint.

• Cast Shoe (FDA Code: IPG / 890.3025)

• Casting Kits, Walkers

• Ceiling Mounted Surgical Light (FDA Code: FSY / 878.4580) A surgical lamp (including a fixture) is a device intended to be used to provide visible illumination of the surgical field or the patient.

• Cement Mixing Equipment (FDA Code: JDZ / 888.4210) A cement mixer for clinical use is a device consisting of a container intended for use in mixing bone cement (888.3027).

• Cement Monomer Vapor Evacuator (FDA Code: JDY / 888.4220) A cement monomer vapor evacuator is a device intended for use during surgery to contain or remove undesirable fumes, such as monomer vapor from bone cement (888.3027).

• Cement Removal Extraction System (FDA Code: LZV / 888.4580) A sonic surgical instrument is a hand-held device with various accessories or attachments, such as a cutting tip that vibrates at high frequencies, and is intended for medical purposes to cut bone or other materials, such as acrylic.

• Cement Restrictor Hip Prosthesis (FDA Code: JDK / 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.

• Cement Ventilation Tube (FDA Code: KII / 888.4230) A cement ventilation tube is a tube-like device usually made of plastic intended to be inserted into a surgical cavity to allow the release of air or fluid from the cavity as it is being filled with bone cement (888.3027).

• Cemented Femoral Components

• Cemented Metal/Polymer + Additive Cemented Semi-Constrained Hip (FDA Code: OQH / 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).

• Cemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: JDI / 888.3350)

• Cemented/Uncemented Semi-constrained Hip Prosthesis (FDA Code: MRA)

• Cementless Acetabular Liners

• Cementless Femoral Components

• Cementless Tibial Components

• Ceramic Acetabular Liners

• Ceramic Semi-Constrained Hip Prosthesis (FDA Code: LPF)

• Cerclage Applier (FDA Code: HXN / 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.

• Cervical Allograft Spacer System

• Cervical Orthosis (FDA Code: IQK / 890.3490) A truncal orthosis is a device intended for medical purposes to support or to immobilize fractures, strains, or sprains of the neck or trunk of the body. Examples of truncal orthoses are the following: Abdominal, cervical, cervical-thoracic, lumbar, lumbo-sacral, rib fracture, sacroiliac, and thoracic orthoses and clavicle splints.

• Cervical Pillow

• Cervical Pillow Roll

• Cervical Thoracic Orthosis (FDA Code: IPT / 890.3490)

• Chisel/Osteotome (FDA Code: KDG / 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.

• Clavicle Splint (FDA Code: IQJ / 890.3490)

• Clip Surgical Applier (FDA Code: GDO / 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.

• Cohesive Elastic Bandage

• Cohesive Elastic Bandage Wrap

• Cold & Hot Packs

• Cold Pack

• Cold Packs/Warm Packs

• Collars

• Colles Fracture Plate

• Compression Hip Screw Systems

• Compression Instrument (FDA Code: HWN / 888.4540)

• Computer-assisted Surgical Systems

• Condylar Plate Fixation Device Implant (FDA Code: JDP / 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.

• Congenital Hip Dislocation Abduction Splint (FDA Code: IOZ / 890.3665) A congenital hip dislocation abduction splint is a device intended for medical purposes to stabilize the hips of a young child with dislocated hips in an abducted position (away from the midline).

• Constrained Elbow Prosthesis (FDA Code: JDC / 888.3150) An elbow joint metal/polymer constrained cemented prosthesis is a device intended to be implanted to replace an elbow joint. It is made of alloys, such as cobalt-chromium-molybdenum, or of these alloys and of an ultra-high molecular weight polyethylene bushing. The device prevents dislocation in more than one anatomic plane and consists of two components that are linked together. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).

• Contour Support Cervical Pillow

• Corkscrew (FDA Code: HWI / 888.4540)

• Countersink (FDA Code: HWW / 888.4540)

• Cranioplasty Plate Fastener (FDA Code: HBW / 882.5360) A cranioplasty plate fastener is a screw, wire, or other article made of tantalum, vitallium, or stainless steel used to secure a plate to the patient's skull to repair a skull defect.

• Crutch (FDA Code: IPR / 890.3150) A crutch is a device intended for medical purposes for use by disabled persons to provide minimal to moderate weight support while walking.

• Crutch and Walker Cane Tips (FDA Code: INP / 890.3790) Cane, crutch, and walker tips and pads are rubber (or rubber substitute) device accessories intended for medical purposes that are applied to the ground end of mobility aids to prevent skidding or that are applied to the body contact area of the device for comfort or as an aid in using an ambulatory assist device.

• Crutches, Canes, Walkers

• Curettes (FDA Code: HTF / 878.4800)