Scient'x USA Inc.

Address: 1015 Maitland Center Commons,Suite 106A, Maitland, Florida 32751, USA
Phone: +1-(,407)-571-2550 | Fax: +1-(407)-571-2551 | Map/Directions >>

Profile: Scient'x USA Inc. offers a wide range of anterior and posterior spinal fixation systems, which include proprietary semi-rigid lumbar system technology, its peek devices, its cervical plate, as well as a unique universal cross link system. Our samarys cervical anterior cage is recommended for the surgical treatment of cervicobrachial neuralgia resulting from disc herniation or compressive osteophytosis, as well as for degenerative intervertebral instabilities.

The company was founded in 2002, has revenues of USD 1-5 Million, has ~20 employees and is CE certified.

32 Products/Services (Click for related suppliers)  
• Awl (FDA Code: HWJ / 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.
• Bender (FDA Code: HXW / 888.4540)
• Bioabsorbable synthetic spacers
• Bone Taps (FDA Code: HWX / 888.4540)
• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)
A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.
• 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.
• 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)
• Guiding Probes
• Laparoscopic Probes
• Laser Power Probe
• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080)
• Medical Probes (FDA Code: HXB / 888.4540)
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Pantheon T Cervical Plate
• PEEK Spacer System
• Periodontal Probes
• Probes (FDA Code: HXB / 888.4540)
• Probes (FDA Code: HXB / 888.4540)
• Removable synthetic spacers
• Rib Rongeurs (FDA Code: HTX / 888.4540)
• Screwdriver (FDA Code: HXX / 888.4540)
• Small Depth Gauge (FDA Code: HTJ / 888.4300)
• Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 888.3050)
A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome.
• Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060)
A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.
• Spinal Pedicle Fixation Orthosis (FDA Code: MNI / 888.3070)
Pedicle screw spinal systems are multiple component devices, made from a variety of materials, including alloys such as 316L stainless steel, 316LVM stainless steel, 22Cr-13Ni-5Mn stainless steel, Ti-6Al-4V, and unalloyed titanium, that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. Such a spinal implant assembly consists of a combination of anchors (e.g., bolts, hooks, and/or screws); interconnection mechanisms incorporating nuts, screws, sleeves, or bolts; longitudinal members (e.g., plates, rods, and/or plate/rod combinations); and/or transverse connectors.
• Spinal Vertebral Body Replacement Device (FDA Code: MQP / 888.3060)
• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)
• Stellar Cervical Plate
• Synthetic Spacers
• Wrench (FDA Code: HXC / 888.4540)

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