Collagen Matrix, Inc. Receives FDA 510(K) Clearance For Synoss Synthetic Mineral Bone Graft Material

Franklin Lakes, NJ - Collagen Matrix, Inc. announces that it has received FDA's 510(k) clearance of its SynOss Synthetic Mineral bone graft material intended for use in oral surgical applications involving bone repair.

SynOss Synthetic Mineral is an osteoconductive calcium phosphate based bone graft material with an apatite structure similar to that of human bone. Unlike hydroxyapatite materials, SynOss' has a carbonate apatite structure which is comparable to the mineralized matrix structure of human bone. The similarity in structure between SynOss and natural bone mineral allows for SynOss' in vivo resorption and remodeling profile to mimic that of natural bone.

The synthetic mineral product is complementary to the Company's existing line of products intended for dental and oral surgery, which include Collagen Dental Membranes, Anorganic Bone Mineral, Anorganic Bone Mineral with Collagen, and Collagen Dental Wound Dressings in various forms (i.e., Foam, Tape, Plug, and Microfibrillar). These products are sold through partnerships with major companies in the dental market.

"Our goal is to provide the dental and oral surgical markets with a full line of innovative products for use in regenerative medicine. The addition of SynOss is another step in reaching that goal," said Shu-Tung Li, Ph.D., Founder and CEO of Collagen Matrix.

SOURCE: Collagen Matrix, Inc.