6,900 results
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41ms
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Sources: EU EUDAMED, US FDA
Restoration, porcelain
FDA registration
V-BEST DENTAL TECHNOLOGY LIMITED·1 product·🇭🇰 Hong Kong
Dentures, partial
FDA registration
V-BEST DENTAL TECHNOLOGY LIMITED·1 product·🇭🇰 Hong Kong
PINSET
FDA 510(k)
FDA Class 2
·Clinical Chemistry
EXIT ALARM
FDA 510(k)
FDA Class 1
·General Hospital
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Master Restore, Itrel®, Synergy®, Intellis and Vanta Spinal Cord Stimulation Systems and Pisces, Specify®, Vectris® S
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·CROSS SAIL CORONARY DILATATION CATHETER
Auto Tono/Refracto/Kerato/Pachymeter HTR-1A
FDA UDI
Huvitz Co., Ltd.·08800019600558·Auto Tono/Refracto/Kerato/Pachymeter HTR-1A
Visionix VX650
FDA UDI
LUNEAU TECHNOLOGY OPERATIONS·03664188000145·
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·CYBERTACH
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH II MODELS 262-16
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH & INTERTACH II PULSE GENERATORS
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·TELECTRONICS PASAR MODEL 4171 PG
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·CYBERTACH PULSE GENERATOR SYSTEM
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH TM IMPLANTABLE PACEMAKER PULSE
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH(R) FAMILY OF PULSE GENERATORS
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH TM IMPLANTABLE PACEMAKER PULSE
Pulse-Generator, Single Chamber, Single
FDA Pre-Market Approval
FDA Class 3
·INTERTACH II MODELS 262-16