— 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 […]
Tesera SA Stand-Alone ALIF Cage System
The Tesera® SA Stand-Alone ALIF Cage is a porous titanium Stand-alone Anterior Cage designed to be part of the fusion, rather than merely a vessel for it. Using additive manufacturing, we have created an ideal trabecular structure for bone in-growth, providing excellent long-term fixation. Four screws and an innovative locking system provide immediate fixation and […]
S128 PEEK ALIF Cage System
The S128 PEEK ALIF Cage is a zero profile Stand-alone Anterior Cage designed for ease of use and patient safety. S128 PEEK ALIF cage Four screws and an innovative locking system provide stability and confidence, and the size array is designed for maximum versatility.
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 […]
Renovis Surgical Announces Partnership with Calvary Spine
— Press Release — Redlands, CA / Austin, TX (December 7, 2010) – Renovis Surgical Technologies, Inc. announced today that it has entered into a strategic partnership with Calvary Spine, LLC, of Baltimore, Maryland. This partnership allows Renovis to distribute the Petra™ and Crescent™ PEEK interbody spacers produced by Calvary Spine. Interbody spacers are used […]