ELECTRO-IMMUNO-QUANTITATION (EIQ)

FDA 510(k)

FDA Class 2 ·Immunology

IBL C1Q-CIC CIA TEST

FDA 510(k)

FDA Class 2 ·Immunology

Complement C1q, Antigen, Antiserum, Control

FDA classification

FDA Class 2 ·Complement C1q, Antigen, Antiserum, Control

NERVEL-NERVE CONDUCTION VELOCITY METER

FDA 510(k)

FDA Class 2 ·Neurology

Vertex Hip Fracture Nailing System

FDA 510(k)

FDA Class 2 ·Orthopedic

Solo+ Tympanostomy Tube Device (TTD)

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube Handpiece (Catalogue #: 12115-100-000) and Solo+ Tympanostomy Tube Cartridge (Catalogue #: 12115-200-000))

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

FIRM MASTER

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/PROXIMITY(TM) INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/C VISTA CERVICAL INTERBODY FUSION DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

FORTAGEN ORAL MEMBRANE

FDA 510(k)

FDA Class 2 ·Dental

SENSOR SHIELD, MODIFICATION

FDA 510(k)

FDA Class 2 ·Cardiovascular

GRAFT PATCH

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SENSOR SHIELD

FDA 510(k)

FDA Class 2 ·Cardiovascular

FORTAFLEX SURGICAL MESH

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery