OptoMonitor System

FDA registration

OPSENS INC.·2 products·🇨🇦 Canada

Opto Wire and OptoMonitor System

FDA 510(k)

FDA Class 2 ·Cardiovascular

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

Hidow TENS/EMS

FDA registration

HI-DOW INTERNATIONAL 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

PROX LAT TIB LK PLT

FDA registration

SYMMETRY MEDICAL THORNTON PRECISION COMPONENTS LTD·1 product·🇬🇧 United Kingdom

Copper Fit Recharge

FDA registration

IDEAVILLAGE PRODUCTS CORP.·2 products·🇺🇸 United States

Hidow TENS/EMS

FDA registration

HI-DOW ELECTRON TECHNOLOGY (HEFEI) INC., LTD·2 products·🇨🇳 China

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

DEFINE

FDA registration

INMODE LTD.·4 products·🇮🇱 Israel

Vienna System

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES

FDA 510(k)

FDA Class 2 ·Orthopedic

HI-DOW-XP

FDA 510(k)

FDA Class 2 ·Neurology

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter