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April 2009

Vidacare appoints Surgical Solutions USA CA distributor for EZ‐IO’s sedation dentistry market.............arrow

Vidacare

November 2008

Wall Street Jounal: Medronic Spinal-Fusions Product Faces an inquiry

Wall Street Journal Health Blog: Feds Probe Unapproved Use of Medtronic Bone Stimulator

September 2008

Osseous Technologies of American announces FDA approval of Collagen Biomaterials LineNewport Beach, CA

Osseous Technologies of America announced today that they have received FDA clearance on their new line of patented Collagen Biomaterials. OTA’s line of Collagen products will be available in a variety of configurations for virtually every application related to pre-prosthetic and bone reconstruction surgery. It provides containment of any type of graft material so that it will not migrate from the placement site. The Socket Capsule, Sinus Capsule, BioSphere and Wedge are intended to be a solution for success for anyone placing dental implants. OTA Collagen Biomaterial is resorbable and intended for placement in the areas of dental implants, bone defects or ridge reconstruction to aid in wound healing post dental surgery. Founded in 2003, Osseous Technologies of America began its current operations to participate in the rapidly expanding dental market for hard and soft tissue products in dental implant surgery. Osseous Technologies of America develops unique, innovative, and economically valued products that address a worldwide market exceeding $2,500,000,000. This dynamic market is fueled by an active aging population and evolving less invasive surgical techniques. OTA is the exclusive vendor of the Balloon for Sinus Lifts and offers a wide range of products and services with the convenience and advantages of an “off the shelf product”.

September 2008

Wall Street Journal: Medtronic Product Linked to Surgery Problems

September 2008

Wall Street Journal: Surgeons With Ties to Medtronic Touted Unapproved Use of Bone Graft

August 2008

Dentistry Today: An Atraumatic Extractor [ Physics Forceps ]: A Biomechanical Rationale by Dr. Carl Misch and Dr. Helena Perez
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July 1st 2008:

FDA Public Health Notification: Life-threatening Complications Associated with Recombinant Human Bone Morphogenetic Protein in Cervical Spine Fusion

April 30th 2008:

Regenaform, Regenafil receives 510(k) NO: K080418
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