19 results
·
43ms
·
Sources: EU EUDAMED, US FDA
Diagon Oblique Cage
FDA registration
CAMBER SPINE TECHNOLOGIES·1 product·🇺🇸 United States
CAMBER SPINE DIAGON OBLIQUE CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
Smith & Nephew, Inc.·00885556600092·MTO ENDSCPC CANN.DRILL BIT 11MM
Axle-X Interspinous Fusion System
FDA registration
Xtant Medical Holdings, Inc.·1 product·🇺🇸 United States
Powder-Free Nitrile Examination Gloves, Blue, Tested for Use With Chemotherapy Drugs
FDA registration
HL RUBBER INDUSTRIES SDN BHD·2 products·🇲🇾 Malaysia
Axle-X spinous fusion system
FDA registration
SUMMIT CITY PRECISION MACHINE·1 product·🇺🇸 United States
Axle-X spinous fusion system
FDA registration
LH MEDICAL CORPORATION·1 product·🇺🇸 United States
HAMMILL MFG. CO.
FDA registration
HAMMILL MFG. CO.·1 product·🇺🇸 United States
MEXPO INTERNATIONAL, INC.
FDA registration
MEXPO INTERNATIONAL, INC.·2 products·🇺🇸 United States
Sochi
FDA UDI
Altus Spine, LLC·00843210167114·Smooth Shaft Polyaxial Screw, 4.0mm x 38mm
Atoll™
FDA UDI
SEASPINE ORTHOPEDICS CORPORATION·10889981052850·4.0mm x 38mm Smooth Shaft Poly Screw Assm. The ...
Remel Cleveland, A Division of Remel Inc.
FDA registration
Remel Cleveland, A Division of Remel Inc.·1 product·🇺🇸 United States
Merz North America, Inc.
FDA registration
Merz North America, Inc.·2 products·🇺🇸 United States
TREK DIAGNOSTIC SYSTEMS, LTD.
FDA registration
TREK DIAGNOSTIC SYSTEMS, LTD.·1 product·🇬🇧 United Kingdom
POWDER-FREE NITRILE EXAMINATION GLOVES, BLUE
FDA 510(k)
FDA Class 1
·General Hospital
BEDSIDE PAEDIATRIC EARLY WARNING SYSTEM (BEDSIDEPEWS)
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Polymer Patient Examination Glove
FDA classification
FDA Class 1
·Polymer Patient Examination Glove