19 results
·
41ms
·
Sources: EU EUDAMED, US FDA
OXFORD
FDA registration
SYMMETRY MEDICAL MANUFACTURING INC.·1 product·🇺🇸 United States
TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEM
FDA registration
Zhejiang Biomet Medical Products Co., Ltd.·1 product·🇨🇳 China
TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEM
FDA registration
BIOMET, INC.·1 product·🇺🇸 United States
OXFORD FIXED LATERAL BEARING PARTIAL KNEE REPLACEMENT (OXFORD TIBIAL TRAYS A-F) IXFORD PARTIAL KNEE REPLACEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
FDA classification
FDA Class 2
·Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943000115·
NextOrtho6517 (LN) - InterFuse T Intervertebral Body Fusion Device
FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States
InterFuse T Intervertebral Body Fusion Device
FDA registration
NEXT ORTHOSURGICAL·1 product·🇺🇸 United States
OSTEOMED
FDA registration
OSTEOMED·1 product·🇺🇸 United States
Sterigenics US LLC
FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States
CORNEAL TREPHINE HANDLE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013223·CORNEAL TREPHINE HANDLE
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943001785·
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943002430·
SANICURE BV
FDA registration
SANICURE BV·1 product·🇳🇱 Netherlands
OverTube Endoscopic Access System
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
INTERFUSE T INVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
OSTEOMED CRANIAL FLAP FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
Plate, Cranioplasty, Preformed, Non-Alterable
FDA classification
FDA Class 2
·Plate, Cranioplasty, Preformed, Non-Alterable
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar