10,000 results · 54ms · Sources: EU EUDAMED, US FDA

TRICON

FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States

TRICON

FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States

Zimmer Biomet Pty Ltd

FDA registration
Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia

TRICON

FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States

ZIMMER PTE. LTD.

FDA registration
ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore

OFFSET TIBIAL TRAY

FDA registration
BIOMET, INC.·1 product·🇺🇸 United States

Zimmer (LN) - OFFSET TIBIAL TRAY

FDA registration
Isomedix Operations, Inc.·1 product·🇺🇸 United States

TRICON

FDA registration
Smith & Nephew, Inc.·1 product·🇺🇸 United States

OFFSET TIBIAL TRAY

FDA registration
Changzhou Biomet Medical Devices Co., Ltd.·1 product·🇨🇳 China

Smith and Nephew

FDA registration
ARVATO USA LLC·1 product·🇺🇸 United States

TRICON

FDA registration
SMITH & NEPHEW, INC.·1 product·🇺🇸 United States

Zimmer (Shanghai) Medical International Trading Co., Ltd.

FDA registration
Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Emblem S-ICD Programmer - Plexus SMT Mfg. Line

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MAESTRO SERIES 500 P.G. MODELS 501, 505, 509

LIPASE DETERMINATION

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

SERUM LIPASE REAGENT SET (TURBIDIMETRIC)

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

TRUCATH.IP

FDA 510(k)
FDA Class 2 ·Immunology