Montage-XT Settable, Resorbable Bone Putty

FDA 510(k)

FDA Class 2 ·Orthopedic

SIGNAFUSE Bioactive Strip (SBS); SIGNAFUSE Putty

FDA 510(k)

FDA Class 2 ·Orthopedic

Morpheus® Moldable; Agilon® Moldable

FDA 510(k)

FDA Class 2 ·Orthopedic

MagnetOs Easypack Putty

FDA 510(k)

FDA Class 2 ·Orthopedic

MERRIES UNI-OSTEO, MODEL CS30250-CS10102

FDA 510(k)

FDA Class 2 ·Orthopedic

Cytomegalovirus (Cmv) Dna Quantitative Assay

FDA classification

FDA Class 2 ·Cytomegalovirus (Cmv) Dna Quantitative Assay

Test, Donor, Cmv

FDA classification

FDA Class 2 ·Test, Donor, Cmv

Resona A10S, Resona A20 Pro, Resona A20T, Resona A20S, Resona A20W, Resona A20, Resona A20 Exp, Resona A20 Premium, Resona A20 Elite, Resona A20 Plus, Resona A Elite, Resona A MV, Eagus A20W, Eagus A20 Diagnostic Ultrasound System

FDA 510(k)

FDA Class 2 ·Radiology

Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv

FDA classification

FDA Class 2 ·Multiplex Flow Immunoassay, T. Gondii, Rubella And Cmv

Attachment, Intermittent Mandatory Ventilation (Imv)

FDA classification

FDA Class 2 ·Attachment, Intermittent Mandatory Ventilation (Imv)

Qualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus Infection

FDA classification

FDA Class 2 ·Qualitative Cytomegalovirus Nucleic Acid-Based Detection Device For Congenital Cytomegalovirus Infection

Ultrasonic Body Composition Analyzer

FDA classification

FDA Class 2 ·Ultrasonic Body Composition Analyzer

Filler, Bone Void, Calcium Compound

FDA classification

FDA Class 2 ·Filler, Bone Void, Calcium Compound

Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2

FDA classification

FDA Class 2 ·Multiplex Immunoassay For T. Gondii, Rubella, Cytomegalovirus And Herpes Simplex Virus 1 And 2

Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm

FDA classification

FDA Class 2 ·Multiplex Flow Immunoassay, T. Gondii, Rubella, Cmv Igm

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