10,000 results
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48ms
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Sources: EU EUDAMED, US FDA
PK Papyrus
FDA UDI
Biotronik AG·07640130447158·
NeoShine
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
disposable mask
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
Zhejiang Letai Optical Glasses Co., Ltd
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
MICROCOPY, DIVISION OF NEO-FLO, INC.
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
Minnow
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
Zhejiang Letai Optical Glasses Co., Ltd
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
Zhejiang Letai Optical Glasses Co., Ltd
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
Reading Glass
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
NeoDiamond IPR Strips
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
Reading Glass
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
NeoDiamond
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
NeoDrys
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
NeoBurr
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
Flaps
FDA registration
MICROCOPY, DIVISION OF NEO-FLO, INC.·1 product·🇺🇸 United States
ACCESSORY, SURGICAL APPAREL
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
Safety goggles
FDA registration
Zhejiang Letai Optical Glasses Co., Ltd·1 product·🇨🇳 China
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Activa® Deep Brain Stimulation Therapy System, Percept PC BrainSense
Stimulator, Electrical, Implantable, For Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim® Therapy System, Verify® Evaluation System
Implanted Electrical Device Intended For Treatment Of Fecal Incontinence
FDA Pre-Market Approval
FDA Class 3
·InterStim® Therapy System, Verify® Evaluation System