CE Mark Approval

Extends SBi’s wrist management portfolio Addresses most common fracture treated by hand surgeons Geometry provides optimized fit for a broad range of anatomic variations

The CYPHER SELECT®Plus Sirolimus-eluting Coronary Stent has received CE marking within the European Union for treatment of patients with diabetes, a complex and often difficult-to-treat patient population.

BIOTRONIK announces the CE mark and completion of the first successful cardiac ablation clinical case with the TRIGNUM Flux magnetic irrigated gold tip catheter.

Aegis Can Now Be Marketed for Use in European Union.
Neovasc Also Announces Senior Management Changes and Issues Options.

PEAK Surgical, Inc., a medical device company that has developed a new tissue dissection system based on a proprietary technology, announced that it has received European CE Mark approval for its PEAK® Surgery System for use in general surgery.

Cardiac Dimensions®, Inc. announced that on January 26th it received the CE Mark approval for its CARILLON™ Mitral Contour System™ from KEMA Quality B.V. – a European Union Notified Body from the Netherlands.

St. Jude Medical, Inc. announced European CE Mark approval of its Libra® and LibraXP™ deep brain stimulation systems for treating the symptoms of Parkinson’s disease, a neurological disorder that progressively diminishes a person’s control over his or her movements and speech.

Adhezion Biomedical LLC announced today that it received European CE Mark (Conformité Européene) approval for FloraSeal, a film-forming, cyanoacrylate-based microbial sealant in a ready-to-use applicator.

Orthomimetics Limited, the UK-Based Regenerative Medicine Company, has Received CE Mark Approval for Chondromimetic, its Flagship Product for the Repair of Articular Cartilage and Bone

Allium Group announced today that it has been awarded CE mark for its prostatic stent enabling commercialization of the system in the European Union and the countries that recognize the CE Mark.

AGA Medical Corporation announced today that it received European CE Mark approval for its AMPLATZER® Cardiac Plug (ACP). The ACP provides an innovative, minimally invasive solution for closing cardiac structures not involving the septal wall.

“Wellex device fills the gap between conservative care and fusion surgery in early-stage degenerative disc disease.”

Guillaume Viallaneix, CEO, Eden Spine

Advanced delivery system gives physicians more control to achieve consistent vascular closure

Alcon, Inc. announced the commercial launch outside the U.S. of the new +3.0 Add Power AcrySof® ReSTOR® Aspheric IOL during the 2008 European Society of Cataract and Refractive Surgeons (ESCRS) meeting in Berlin, Germany

Baxter’s COSEAL Surgical Sealant gets CE marked and launched.