19 results
·
41ms
·
Sources: EU EUDAMED, US FDA
DEFINE
FDA registration
INMODE LTD.·4 products·🇮🇱 Israel
DEFINE System (AG612444A)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Massager, Vacuum, Radio Frequency Induced Heat
FDA classification
FDA Class 2
·Massager, Vacuum, Radio Frequency Induced Heat
PERI LOCKING SCREW 3.5MM X 46MM, NON-STERILE
FDA registration
SYNTEC SCIENTIFIC CORP.·2 products·🇹🇼 Taiwan
Zimmer Biomet Pty Ltd
FDA registration
Zimmer Biomet Pty Ltd·2 products·🇦🇺 Australia
Periarticular Locking Plates and Screws, 2357 and 2359 series
FDA registration
ZIMMER, INC.·2 products·🇺🇸 United States
Periarticular Locking Plate System
FDA registration
MAITLAND ENGINEERING·1 product·🇺🇸 United States
Zimmer (Shanghai) Medical International Trading Co., Ltd.
FDA registration
Zimmer (Shanghai) Medical International Trading Co., Ltd.·2 products·🇨🇳 China
OptoMonitor System
FDA registration
OPSENS INC.·2 products·🇨🇦 Canada
PROX LAT TIB LK PLT
FDA registration
SYMMETRY MEDICAL THORNTON PRECISION COMPONENTS LTD·1 product·🇬🇧 United Kingdom
Periarticular Locking Plates and Screws, 2357 and 2359 series
FDA registration
Sterigenics US, LLC·2 products·🇺🇸 United States
PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES
FDA registration
BIOMET CHILE S.A.·2 products·🇨🇱 Chile
ZIMMER PTE. LTD.
FDA registration
ZIMMER PTE. LTD.·2 products·🇸🇬 Singapore
Viant Medical, LLC
FDA registration
Viant Medical, LLC·2 products·🇺🇸 United States
Synergy Health AST, SRL
FDA registration
Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica
PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
Opto Wire and OptoMonitor System
FDA 510(k)
FDA Class 2
·Cardiovascular
Wire, Guide, Catheter
FDA classification
FDA Class 2
·Wire, Guide, Catheter
Plate, Fixation, Bone
FDA classification
FDA Class 2
·Plate, Fixation, Bone