5,326 results · 31ms · Sources: EU EUDAMED, US FDA

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·TECHNICON-38 POLYMACON HYDROPHILIC LENS

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·KONTUR SOFT (METHAFILCON A) CONTACT LNS

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA Pre-Market Approval
FDA Class 2 ·GORE-TEX(R) SUTURE

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA Pre-Market Approval
FDA Class 2 ·GORE-TEX(TM) SUTURE

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·FLEXLENS (HEFILCON A) SOFT CONTACT LENSES

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA Pre-Market Approval
FDA Class 2 ·GORE-TEX(TM) SUTURE

Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA Pre-Market Approval
FDA Class 2 ·HEALTHTRONICS LITHOTRON LIHTOTRIPSY SYSTEM

System, Nuclear Magnetic Resonance Imaging

FDA Pre-Market Approval
FDA Class 2 ·NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS

System, Nuclear Magnetic Resonance Imaging

FDA Pre-Market Approval
FDA Class 2 ·NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval
FDA Class 2 ·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS

Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA Pre-Market Approval
FDA Class 2 ·STORZ MODULITH LITHOTRIPTER, MODEL SLX

Bone Cement

FDA Pre-Market Approval
FDA Class 2 ·OSTEOPAL

Lithotriptor, Extracorporeal Shock-Wave, Urological

FDA Pre-Market Approval
FDA Class 2 ·STORZ TRANSPORTABLE MODULITH SLX LITHOTRIPTER VERSION) ANSPORTABLE VERSION)

Lenses, Soft Contact, Daily Wear

FDA Pre-Market Approval
FDA Class 2 ·KONTUR SOFT (METHAFILCON A) LENS

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA Pre-Market Approval
FDA Class 2 ·GORE-TEX SUTURE WITH PLEDGETS

System, Nuclear Magnetic Resonance Imaging

FDA Pre-Market Approval
FDA Class 2 ·NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

System, Nuclear Magnetic Resonance Imaging

FDA Pre-Market Approval
FDA Class 2 ·NUCLEAR MAGNETIC RESONANCE SCANNER MODELS NMR 1000