24 results · 34ms · Sources: EU EUDAMED, US FDA

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T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing System

FDA 510(k)
FDA Class 2 ·Orthopedic

ARTiC-L™ Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000085384·TRIAL 5251400 L 25 HT 14 DEG 0 FIXED

ARTiC-L™ 3D Ti Spinal System with TiONIC™ Technology

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169791114·TRIAL 5251400 L 25 HT 14 DEG 0 FIXED

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613115012·Freer Skin Hook, 2 Prongs, Sharp, Overall Lengt...

XiVE®

FDA UDI
Dentsply Implants Manufacturing GmbH·EFRI322514002·XiVE® TG Cover Screw for Implants

XiVE®

FDA UDI
Dentsply Implants Manufacturing GmbH·07392532223105·XiVE® TG Cover Screw for Implants

IdentiTi

FDA UDI
ALPHATEC SPINE, INC.·00190376116723·LLIF Inst, Graft Containment Slide, 14mm, 0°

IdentiTi

FDA UDI
ALPHATEC SPINE, INC.·00190376383514·LIF, GRAFT CONTAINMENT CLIP, 14MM 0°

IPL HAIR REMOVAL DEVICE CT05

FDA Adverse Event
Injury ·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·February 19, 2026

HAND-HELD HAIR REMOVAL DEVICE

FDA Adverse Event
Injury ·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·March 9, 2026

Ergoline, Sun Angel, Soltron, Sundash and Palm Beach Tan Sunlamp Products

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

DATEX-OHMEDA S/5 ANESTHESIA MONITOR WITH L-ANEO5 AND L-ANEO5A SOFTWARE, USING F-CU8 OR F-CU5(P) MONITOR FRAME OPTIONS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Omnia Medical TiBrid™-L

FDA UDI
OMNIA MEDICAL, LLC·00843511106508·LATERAL INTERBODY, 22x45x14mm, 0°

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·September 9, 2025

SYNERGY XD

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 22, 2024

TRUETRACK

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·January 2, 2018

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·November 14, 2014

ANEURX AAADVANTAGE STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 13, 2011

ACCU-CHEK D-TRONPLUS

FDA Adverse Event
Malfunction ·ROCHE HEALTH SOLUTIONS, INC·Product code LZG·July 29, 2013

OMNIPOD INSULIN PUMP

FDA Adverse Event
Malfunction ·INSULET CORP·Product code LZG·June 1, 2007