21 results
·
46ms
·
Sources: EU EUDAMED, US FDA
Catheter 3Fr or 4Fr and Guide
FDA registration
Kitazato Corporation·1 product·🇯🇵 Japan
Stylet for Guide
FDA registration
STERI-TECH CO.,LTD.·1 product·🇯🇵 Japan
Stylet for Guide
FDA registration
KITAZATO CORPORATION·1 product·🇯🇵 Japan
Kitazato ET Catheters
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Catheter, Assisted Reproduction
FDA classification
FDA Class 2
·Catheter, Assisted Reproduction
Phasix Mesh
FDA UDI
Davol Inc.·00801741107658·Phasix™ Mesh
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169599314·TRIAL 2192540 O25 IB 27MM 12 DEG 16X40
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
ROMD, LLC
FDA registration
ROMD, LLC·1 product·🇺🇸 United States
InterPlate Spacer L-PS
FDA registration
RSB SPINE LLC.·2 products·🇺🇸 United States
Greatbatch Medical
FDA registration
Greatbatch Medical·1 product·🇺🇸 United States
OIC CERVICAL CAGE
FDA registration
THE ORTHOPAEDIC IMPLANT COMPANY·2 products·🇺🇸 United States
Greatbatch Medical, S. de R.L. de C.V.
FDA registration
Greatbatch Medical, S. de R.L. de C.V.·1 product·🇲🇽 Mexico
Isomedix Operations, Inc.
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
Aneroid sphygmomanometer(HS-20A, HS-20D,HS-201W,HS-201Y,HS-201C1,HS-201Q3,HS-50B,HS-50C,HS-50D
FDA registration
HONSUN (NANTONG) Co., Ltd.·2 products·🇨🇳 China
EXPERIENCE
FDA UDI
Gc Orthodontics America Inc.·D78819254000071·Exp CCO RH 022/U4&5 -9T 0A
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78819254000201·EXMRC MBT 022/U4 & 5 UNIV - 7T 0A
C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
PTFE PORTABLE INTRODUCER
FDA 510(k)
FDA Class 2
·Cardiovascular
Intervertebral Fusion Device With Bone Graft, Cervical
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Cervical