18 results
·
50ms
·
Sources: EU EUDAMED, US FDA
Bio-logic AuDX Pro
FDA registration
NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK)·1 product·🇨🇦 Canada
AUDX PRO OTOACOUSTIC EMISSIONS MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Navigation Panel Unit
FDA registration
KARL STORZ SE & CO KG·1 product·🇩🇪 Germany
HEADBAND, SINGLE USE
FDA registration
JOSEF FRECH GMBH & CO. KG·1 product·🇩🇪 Germany
Millstone Medical Outsourcing LLC
FDA registration
Millstone Medical Outsourcing LLC·3 products·🇺🇸 United States
Navigation Panel Unit
FDA registration
KARL STORZ SE & CO. KG·1 product·🇩🇪 Germany
Navigation Panel Unit
FDA registration
Karl Storz Endoscopy-America, Inc.·1 product·🇺🇸 United States
Navigation Panel Unit
FDA registration
KARL STORZ SE & CO. KG·1 product·🇩🇪 Germany
Cross-Fuse II PEEK IBF System
FDA registration
Xtant Medical Holdings, Inc.·3 products·🇺🇸 United States
KARL STORZ
FDA registration
KARL STORZ ENDOSCOPY CANADA LTD.·1 product·🇨🇦 Canada
Audiometer
FDA classification
FDA Class 2
·Audiometer
Supercath5
FDA registration
TOGO MEDIKIT CO., LTD.·1 product·🇯🇵 Japan
Topical Tissue Adhesives
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India
Arthrosurface® Total Toe - Proximal Phalanx Implant
FDA registration
ARTHROSURFACE, INC.·1 product·🇺🇸 United States
PIONEER CROSSFUSE II IBF/VBR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS
FDA 510(k)
FDA Class 3
·Cardiovascular
Automated External Defibrillators (Non-Wearable)
FDA classification
FDA Class 3
·Automated External Defibrillators (Non-Wearable)
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar