G Surgical Co., Ltd.

Contact: Donald Grafton
Web: http://www.gsurgical.com
Address: 152 Soi Ramkhamhaeng 138, Sapansung, Bangkok 10240, Thailand
Phone: +66-(22)-7306288 | Fax: +66-(22)-7306287 | Map/Directions >>

Profile: G Surgical Co., Ltd. deals with medical products. Our products are lumbar and cervical thoracic system. We provide surgical pedicle system, which features a low profile, polyaxial and monoaxial self tapping screw system for the treatment of severe spondylolisthesis. Our anterior lumbar stabilization system is a low profile one and two level plate, with preformed lordotic radius and cancellous locking screws. We supply Gsurgical pedicle system, which features polyaxial design and small size for precise placement and fusion of the cervical and thoracic spine. We also provide anterior cervical plate system, which is a multilevel plates system, large visualization windows and low profile design for anterior cervical spine.

FDA Registration Number: 3006378738
US Agent: Donald Grafton / G Surgical Llc
Phone: +1-(318)-670-1100 Fax: +1-(318)-670-1100 E-Mail:

9 Products/Services (Click for related suppliers)

• Cervical Plate System

• General Surgical Manual Instrument (FDA Code: MDM / 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.

• Lumbar

• Pedicle Screw System

• 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 Pedicle Screw Fixation Appliance System (FDA Code: MCV)

• Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070)