News

Renovis Surgical Receives FDA Clearance for 3D-printed Posterior Lumbar Interbody Fusion Systems

— Press Release — Redlands, CA / Austin, TX (August 9, 2017) – Renovis Surgical Technologies, Inc. announced today that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market posterior lumbar Tesera® porous titanium interbody fusion systems. These systems feature implants for direct posterior (PLIF) or transforaminal (TLIF) approaches […]

Renovis Surgical Receives FDA Clearance for First-ever 3D Printed Titanium Stand-alone Cervical Cage

— 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 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 […]

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 […]

Renovis Surgical Releases Hip Replacement System with Vitamin E Polyethylene

— Press Release — Redlands, CA / Austin, TX (June 13, 2012) – 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 A450 Acetabular Cup and A400 Tapered Cementless Hip Stem. This new line of hip replacement implants includes versatile femoral […]

Renovis Surgical Announces FDA Clearance of T700 Cannulated Screw System

— Press Release — Redlands, CA / Austin, TX (December 9, 2011) – 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 T700™ Cannulated Screw system. As the first offering in the company’s trauma product line, this marks a major milestone […]

Renovis Surgical Obtains ISO 13485:2003 Certification Supports Commitment to Quality Systems

— Press Release — Redlands, CA / Austin, TX (September 7, 2011) – Renovis Surgical Technologies, Inc. a manufacturer of medical devices, today announced that it had received ISO 13485:2003 quality management system certification from BSI Group America Inc. for both its Redlands and Austin facilities. This certification emphasizes meeting regulatory and customer requirements, risk […]

Renovis Surgical Announces FDA Clearance of T710 External Fixation System

— Press Release — Redlands, CA / Austin, TX (May 11, 2011) – 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 T710™ Large External Fixation System. The T710 External Large Fixation System was designed to temporarily stabilize fractures in the […]

Renovis Surgical Announces FDA Clearance of S100 Spine System

— Press Release — Redlands, CA / Austin, TX (December 7, 2010) – 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 S100™ Pedicle Screw System. This full-featured thoracolumbar pedicle screw and rod system is used to treat various degenerative conditions […]