5,326 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
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