10,000 results
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47ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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VELOX ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ELECTRO-CAP SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
OSTEOPORE TCP
FDA 510(k)
FDA Class 2
·Orthopedic
3M CURING LIGHT XL1500
FDA 510(k)
FDA Class 2
·Dental
ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System
FDA 510(k)
FDA Class 2
·Neurology
XSTAT 30 Pouch
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Disposable EEG Electrodes (MODEL: DL, E-CAP, FLEX-CAP)
FDA 510(k)
FDA Class 2
·Neurology
COSGROVE DEPTH ELECTRODE KIT(CDEK)
FDA 510(k)
FDA Class 2
·Neurology
OPERATING ARM SYSTEM (OAS) [WITH CT AND MR IMAGES]
FDA 510(k)
FDA Class 2
·Neurology
ELI 250 ELECTROCARDIOGRAPH
FDA 510(k)
FDA Class 2
·Cardiovascular
OPTICAL TRACKING SYSTEM (OTS)
FDA 510(k)
FDA Class 2
·Neurology
PACE-1A CARDIAC STIMULATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI PROBE III BALLOON-ON-A-WIRE DILATATION SYSTEM
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·\EART TRAK,HART TRAK III,MAX TRAK,MAX TRAK DP,PROA
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·DISINTEGRATOR PRO NEEDLE DESTRUCTION DEVICE
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·GELFLEX(R) (DIMEFILCON A) CONTACT LENS