Hexanium® TLIF

FDA registration

FMI MEDISCH BV·1 product·🇳🇱 Netherlands

Intervertebral Fusion Device with Bone Graft, Lumbar

FDA registration

SIMON SAS·1 product·🇫🇷 France

SPINEVISION SAS

FDA registration

SPINEVISION SAS·1 product·🇫🇷 France

Synergy Health Marseille SAS

FDA registration

Synergy Health Marseille SAS·1 product·🇫🇷 France

SIMAGEC

FDA registration

SIMAGEC·1 product·🇫🇷 France

Hexanium® TLIF

FDA 510(k)

FDA Class 2 ·Orthopedic

BI-METRIC XR-SERIES HIP SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304650619·

Maestro™ Total Wrist

FDA UDI

Biomet Orthopedics, LLC·00887868240089·

MAESTRO TOTAL WRIST

FDA UDI

Biomet Orthopedics, LLC·00880304555242·

MICRUS MICROCOIL SYSTEM, "DELTAPAQ 10 CERECYTE", MODEL CDF

FDA registration

MEDOS INTERNATIONAL SARL·1 product·🇨🇭 Switzerland

Su-Por Surgial Implant

FDA registration

PORIFEROUS, LLC·2 products·🇺🇸 United States

ANDREWS PYNCHON SUCTION TUBE

FDA UDI

SONTEC INSTRUMENTS, INC.·B0991804370·ANDREW PYNCHON SUCTION TUBE CHROME

BI-METRIC XR-SERIES HIP SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304650282·

RESMED CORP

FDA registration

RESMED CORP·1 product·🇺🇸 United States

Silicone Punctum Plug

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF

FDA 510(k)

FDA Class 2 ·Neurology

AP-1000 BLOOD GLUCOSE MONITORING SYSTEM, MODEL AP-1000, MAJOR GLUCOSE CONTROL SOLUTION

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Device, Neurovascular Embolization

FDA classification

FDA Class 2 ·Device, Neurovascular Embolization

System, Test, Blood Glucose, Over The Counter

FDA classification

FDA Class 2 ·System, Test, Blood Glucose, Over The Counter