Sequel - Orthoplastic Tool
The Only Company that brings you a complete portfolio for your orthoplastic needs.
Product Details
WOUND DEBRIDEMENT
SonicOne is the only debridement tool with aspiration you can use directly over sensitive structures without damaging them12. The ultrasonic technology accurately debrides unhealthy tissue. A cleaner wound bed means preserving healthy tissue to promote more healing1,2.
TheraGenesis Bilayer Wound Matrix is a collagen-based wound dressing that consists of two layers: a porcine tendon-derived atelocollagen sponge layer and a silicone film layer. It contains a non-adhesive gauze (TREX™) to reinforce the silicone film. The meshed type has slits to aid in the drainage of exudate. The biodegradable collagen matrix provides a scaffold for cellular invasion and capillary growth.
Introducing Sequel External Ring Fixation System. We have concentrated the best of our existing technologies into the foot and ankle markets for a comprehensive approach to limb salvage. We see this as a three-step process each with excellent technologies to help surgeons achieve predictable optimal clinical outcomes.
The Sequel™ External Fixation System is indicated for both adult and pediatric patients for:
- Open and closed fracture fixation
- Pseudoarthrosis or non-union of long bones
- Limb lengthening by epiphyseal or metaphyseal distraction
- Correction of bony or soft tissue deformities
- Correction of segmental or nonsegmental bony or soft tissue defects
- Post-Traumatic joint contracture resulting in the loss of range of motion.
The Sequel™ External Fixation System is contraindicated for:
- Clinical cases where there is an active infection.
- Patients conditions that limit blood supply or where there is insufficient quality or quantity of bone.
- Patients with mental or neurologic conditions who are unwilling or incapable of following postoperative care instructions.
- Cases where foreign body sensitivity or component material sensitivity is suspected. In such cases, sensitivity testing is to be conducted prior to implantation of the device.
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