Tecomet, Inc.

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Contact: Pat O'Neill - Vice President
Web: http://www.tecomet.com
E-Mail:
Address: 170 New Boston St., Woburn, Massachusetts 01801, USA
Phone: +1-(781)-782-6400 | Fax: +1-(781)-933-8872 | Map/Directions >>

Profile: Tecomet, Inc. designs, develops, and manufactures orthopedic implants for surgical reconstruction & revision, trauma, spinal and cranio-maxillofacial applications. We are accredited with ISO 9001:2000, and ISO 13485:2003 certifications. Our engineering process is driven by Unigraphics NX, one of the most sophisticated 3D CAD/CAM systems in the industry. Our exclusive photo etching technology provides the foundation for top quality titanium trauma and reconstruction mesh implants. The virtually unlimited range of designs, patterns and thicknesses of the implants allow applications specific to cranial and maxillofacial surgery, neurosurgery, otolaryngology, and plastic surgery. We produce spinal cages, spacers, plates, cervical and lumbar discs for spinal surgery.

The company was founded in 1995, has revenues of USD 10-25 Million, has ~180 employees and is ISO 9002 certified. NYSE:VAS (SEC Filings)

FDA Registration Number: 1225675

20 Products/Services (Click for related suppliers)

• Battery-Powered Thermal Soft-Lens Sterilizer (FDA Code: HRC / 886.5928)

A soft (hydrophilic) contact lens care product is a device intended for use in the cleaning, rinsing, disinfecting, lubricating/rewetting, or storing of a soft (hydrophilic) contact lens. This includes all solutions and tablets used together with soft (hydrophilic) contact lenses and heat disinfecting units intended to disinfect a soft (hydrophilic) contact lens by means of heat.

• 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.

• Burr Hole Cover (FDA Code: GXR / 882.5250)

A burr hole cover is a plastic or metal device used to cover or plug holes drilled into the skull during surgery and to reattach cranial bone removed during surgery.

• Cervical and Lumbar Discs

• Cobalt Chrome Hip Systems

• Contract Manufacturing

• Knee Joint Femorotibial Metal/Polymer Non-constrained Cemented Prosthesis (FDA Code: HSX / 888.3520)

A knee joint femorotibial metal/polymer non-constrained cemented prosthesis is a device intended to be implanted to replace part of a knee joint. The device limits minimally (less than normal anatomic constraints) translation in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral condylar resurfacing component or components made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components made of ultra-high molecular weight polyethylene and are intended for use with bone cement (888.3027).

• Knee Systems

• 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.

• Orthopaedic Implants

• Polymer/Metal/Polymer Cemented Semi-Constrained Partial Knee Patellofemorotibial Prosthesis (FDA Code: NPJ / 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).

• Reconstruction Mesh Implants

• Semi-Constrained Patellofemoral Knee Prosthesis (FDA Code: KRR / 888.3540)

A knee joint patellofemoral polymer/metal semi-constrained cemented prosthesis is a two-part device intended to be implanted to replace part of a knee joint in the treatment of primary patellofemoral arthritis or chondromalacia. 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 a component made of alloys, such as cobalt-chromium-molybdenum or austenitic steel, for resurfacing the intercondylar groove (femoral sulcus) on the anterior aspect of the distal femur, and a patellar component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those devices intended for use with bone cement (888.3027). The patellar component is designed to be implanted only with its femoral component.

• Semi-Constrained Patellofemorotibial Knee Prosthesis (FDA Code: JWH / 888.3560)

• Spinal Cages

• Spinal Plates

• Spinal Spacers

• Stainless Steel Hip Systems

• Zirconium Femoral Component