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