MagnetOs

FDA 510(k)

FDA Class 2 ·Orthopedic

MagnetOs granules

FDA 510(k)

FDA Class 2 ·Orthopedic

AttraX Putty

FDA 510(k)

FDA Class 2 ·Orthopedic

MagnetOs Flex Matrix

FDA 510(k)

FDA Class 2 ·Orthopedic

DYNAGRAFT II

FDA 510(k)

FDA Class 2 ·Orthopedic

MagnetOs MIS

FDA 510(k)

FDA Class 2 ·Orthopedic

ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY

FDA 510(k)

FDA Class 2 ·Dental

MagnetOs Putty

FDA 510(k)

FDA Class 2 ·Orthopedic

Anti-Mutated Citrullinated Vimentin Igg

FDA classification

FDA Class 2 ·Anti-Mutated Citrullinated Vimentin Igg

Syringe, Balloon Inflation

FDA classification

FDA Class 2 ·Syringe, Balloon Inflation

Bone Cement, Antibiotic

FDA classification

FDA Class 2 ·Bone Cement, Antibiotic

Syringe, Balloon Inflation, Exempt

FDA classification

FDA Class 2 ·Syringe, Balloon Inflation, Exempt

Nucleic Acid Amplification Test For The Quantitation Of Epstein-Barr Virus (Ebv) Dna

FDA classification

FDA Class 2 ·Nucleic Acid Amplification Test For The Quantitation Of Epstein-Barr Virus (Ebv) Dna

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535