DDU-1000 Semiautomatic External Defibrillator and Accessories

FDA registration

DEFIBTECH LLC·1 product·🇺🇸 United States

DDU-1000 Semiautomatic External Defibrillator and Accessories

FDA registration

Defibtech Branford·1 product·🇺🇸 United States

DDU-1000 Semiautomatic External Defibrillator and Accessories

FDA registration

DEFIBTECH, LLC·1 product·🇺🇸 United States

SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES

FDA 510(k)

FDA Class 3 ·Cardiovascular

Perimeter TI

FDA registration

WARSAW ORTHOPEDIC, INC.·1 product·🇺🇸 United States

Bacfuse 8 & 10mm

FDA registration

SURGENTEC LLC·1 product·🇺🇸 United States

Perimeter TI

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

Perimeter TI

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167311315250·

TALOS° HA PEEK IBF

FDA UDI

MEDITECH SPINE, LLC·B167321315250·

ORCHID ORTHOPEDICS SWITZERLAND GMBH

FDA registration

ORCHID ORTHOPEDICS SWITZERLAND GMBH·1 product·🇨🇭 Switzerland

xTAG CYP2C19 KIT V3

FDA registration

LUMINEX MOLECULAR DIAGNOSTICS, INC.·1 product·🇨🇦 Canada

KinematX

FDA registration

JANCO, INC.·1 product·🇺🇸 United States

BENCHMARK ELECTRONICS, INC.

FDA registration

BENCHMARK ELECTRONICS, INC.·1 product·🇺🇸 United States

PIONEER SPINOUS PROCESS FUSION PLATE

FDA 510(k)

FDA Class 2 ·Orthopedic

PERIMETER INTERBODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

Appliance, Fixation, Spinal Interlaminal

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Interlaminal

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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