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