— Press Release — Redlands, CA / Austin, TX (March 30, 2016) – Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera™ SC – Porous Titanium Cervical Interbody Fusion System. Tesera SC is a porous titanium stand-alone cervical interbody fusion […]
Renovis Surgical Receives FDA Clearance for First-ever 3D Printed Titanium Stand-alone Cervical Cage
Tesera SC Stand-Alone Cervical Interbody System
The Tesera® SC Stand-Alone Cervical Interbody Fusion System combines our most advanced material science and revolutionary manufacturing process into a powerful stand-alone cervical interbody fusion system. Using additive manufacturing, we have created an ideal trabecular structure for bone in-growth, providing excellent long-term fixation. Three screws and an innovative locking system provide immediate fixation and confidence. […]
Tesera Trabecular Technology Acetabular System
Features and Benefits
Tesera Trabecular Technology Highly porous, with large interconnected pores (average pore diameter about 500 µm) Produced from “gold-standard” titanium alloy Not a coating: Solid and porous portions produced in one manufacturing step Learn more about Tesera Trabecular Technology. Multiple advanced bearing options 28, 32, 36 and 40mm head diameters CoCr and BIOLOX®† delta ceramic femoral […]
Renovis Surgical Receives FDA Clearance for Tesera Trabecular Technology™ Acetabular Devices
— Press Release — Redlands, CA / Austin, TX (April 15, 2014) – Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera Trabecular Technology™ Acetabular System. This novel hip implant is manufactured utilizing additive manufacturing and a patent-pending design to […]
Renovis Surgical Received FDA Clearance of Porous Titanium Spinal Implant
— Press Release — Redlands, CA / Austin, TX (October 3, 2013) – Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera™ Stand-alone ALIF Cage. This titanium implant uses additive manufacturing and a patent-pending design to create porous surfaces that […]
S128 PEEK ALIF Cage System Sizes and Specs
Dimensions 30mm(W) x 26mm(D) 34mm(W) x 28mm(D) 38mm(W) x 30mm(D) 7 Degree Lordosis 11 11 11 13 13 13 15 15 15 17 17 17 19 19 19 12 Degree Lordosis 11 11 11 13 13 13 15 15 15 17 17 17 19 19 19 Graft Chamber Part Number Width Depth Height Lordosis Graft […]
S128 PEEK ALIF Cage System Features and Benefits
The S128 ALIF Cage is a zero profile Stand-alone Anterior Cage designed for ease of use and patient safety. Some text highlighting a feature. Locking Cover Plate A quarter turn is all that it takes to lock all four screws. And with tactile and visual confirmations, you can be confident the system is locked before […]
Tesera SA Features and Benefits
The Tesera ALIF Cage features an ideal trabecular structure for bone in-growth, providing excellent long-term fixation. Truly porous Using additive manufacturing, the entire cage is “grown” layer upon layer, in much the same fashion as traditional rapid prototyping, but instead of plastic, we use titanium alloy powder. The final product is a solid structure in […]
Tesera SA Sizes and Specs
Dimensions
Renovis Surgical Releases Knee Replacement System with Vitamin E Polyethylene
— Press Release — Redlands, CA / Austin, TX (February 14, 2013) – Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the A200 Cruciate Retaining Total Knee System. This new knee system was designed for anatomic fit and long-term performance and […]