— 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 […]