22 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Sterigenics US LLC
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
Endoskeleton TT IBD
FDA registration
PERRYMAN COMPANY·1 product·🇺🇸 United States
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA registration
Medtronic Distribution Center·1 product·🇺🇸 United States
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA registration
Titan Spine, a Division of Medtronic·1 product·🇺🇸 United States
ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD)
FDA 510(k)
FDA Class 2
·Orthopedic
appliance, fixation, nail/blade/plate combination, multiple component Reprocessed External Fixation Devices
FDA registration
Sterigenics US LLC·3 products·🇺🇸 United States
Isomedix Operations Inc.
FDA registration
Isomedix Operations Inc.·1 product·🇺🇸 United States
Reprocessed External Fixation Device
FDA registration
Stryker Sustainability Solutions·3 products·🇺🇸 United States
Reprocessed External Fixation Device
FDA registration
Stryker Sustainability Solutions Phoenix·3 products·🇺🇸 United States
Pronto LP Extraction Catheter. Model number 5010 - PRONTO LP 6F
FDA registration
Teleflex Medical de Tecate, S. de R.L de C.V.·1 product·🇲🇽 Mexico
Ag Positive Control ELISA
FDA registration
MONOCENT INC.·1 product·🇺🇸 United States
BinaxNOW Malaria Positive Control
FDA registration
Abbott Diagnostics Scarborough, Inc.·1 product·🇺🇸 United States
VASCULAR SOLUTIONS LLC
FDA registration
VASCULAR SOLUTIONS LLC·1 product·🇺🇸 United States
BinaxNOW Malaria Positive Control
FDA registration
ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·1 product·🇺🇸 United States
CODAN US I.V. ADMINISTRATION SET, MODEL B400 SP
FDA 510(k)
FDA Class 2
·General Hospital
OSSTELL RESONANCE FREQUENCY ANALYZER
FDA 510(k)
FDA Class 1
·Dental
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar