54 results · 22ms · Sources: EU EUDAMED, US FDA

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Axis Spine Technologies ALIF

FDA 510(k)
FDA Class 2 ·Orthopedic

Laminated Mesh

FDA UDI
TP ORTHODONTICS INC·00192029050521·Molar Bonding Base

Inertia® Pedicle Screw and Deformity Correxxion® System

FDA UDI
NEXXT SPINE, LLC·00889929027301·MAC Pedicle Screw, Ø10.5x90 mm

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197522458·Infero-Posterior Acetabular Capsul...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197522441·Infero-Posterior Acetabular Capsul...

EUROPA™ Pedicle Screw

FDA UDI
MIRUS LLC·00810025483104·Ø10.5 X 90mm EUROPA™ Pedicle Screw

NEUROPACK MICRO, MODEL MED-9100A SERIES

FDA 510(k)
FDA Class 2 ·Physical Medicine

INTRABEAM NEEDLE APPLICATOR

FDA 510(k)
FDA Class 2 ·Radiology

ALINITY I TOXO IGG REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·March 31, 2026

ARCHITECT TOXO IGG

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·April 27, 2026

ARCHITECT TOXO IGG

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·March 19, 2026

LPS DISASSEMBLY TOOL

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·October 22, 2008

INSTATRAK 3500

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 8, 2011

ATLAS II PLUS DR

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 8, 2013

ALINITY I TOXO IGG REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·April 8, 2026

ALINITY I TOXO IGG REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·March 4, 2026

ALINITY I TOXO IGG REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·April 2, 2026

ARCHITECT TOXO IGG

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·July 31, 2025

ARCHITECT TOXO IGG

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·November 10, 2025

ALINITY I TOXO IGG

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code LGD·July 14, 2025