About Us

Unicare Biomedical, Inc.’s mission is to provide scientifically sound and high quality medical products for the healthcare community. The Company focuses on the development and supply of wound care and tissue regeneration products for dental and orthopedic applications. These products facilitate bone regeneration and the management of bleeding as a result of surgical operations or traumatic injuries.

MORE THAN 20 YEARS SERVING THE MEDICAL INDUSTRY

1999

Unicare Biomedical became incorporated and entered the growing field of implant dentistry.

1999

2000

Sets out manufacture of the first FDA cleared bone grafting material, Unigraft®, for use in the reconstruction of extraction sites and alveolar ridge reconstruction.

2000

2001

Introduction of Cytoflex® Tef-Guard®, the novel micro-porous ePTFE barrier membrane for use in guided tissue regeneration procedures. The non-resorbable micro-porous barrier was specifically designed to improve flap attachment while preventing new tissue and bacteria penetration.

2001

2002

Cytoflex® Mesh, the golden precision titanium mesh, receives clearance by the FDA for the fixation of bone grafting material. The mesh is less intrusive, easy to trim, and shapes easily into three-dimensional contours for the containment of bone graft material.

2002

2008

BenaCel®, a resorbable hemostatic wound dressing is approved for the management of bleeding wounds. Its exceptional hemostatic ability makes it perfect for addressing surgical wounds and traumatic injuries.

2008

2009

Further FDA clearance of BenaCel® dental dressing in the management of alveolar osteitis (dry socket) in extraction sites, and for the management of oral surgical wounds, proving the broad applications of BenaCel® hemostatic wound care products.

2009

2009

Introduction of Cytoflex® Resorb, a micro-porous, synthetic resorbable membrane for guided tissue regeneration applications. The poly(lactide-co-glycolide) resorbable barrier gradually dissolves over a 90 day period and does not require a second retrieval procedure.

2009

2013

Textured Cytoflex® Tefguard®, a textured version of our initial non-resorbable micro-porous barrier, is introduced for GTR/GBR applications. The patent pending textured barrier provides micro and macro texture on both surfaces to enhance flap attachment.

2013

2015

Cytoflex® Titanium Mesh is improved upon by increasing the firmness of the material and adding a reinforced edge, while still providing optimal flexibility when shaping for intricate contours. The new M4 model mesh contains pure titanium and a distinct golden color for a more aesthetic compatibility with a patient’s gingiva.

2015

2016

Introduction of Ti-Enforced™, a Titanium-reinforced, multi-layer, ePTFE membrane, designed for more secure graft containment during wound healing as well as to provide a favorable environment for bone regeneration to the desired contour. The bacteria blocking, Ti-Enforced™ ePTFE membrane has a thin and easily conformable profile facilitating bone regeneration for the most demanding conditions.

2016

Quality

Innovate

Responsibility