18 results · 31ms · Sources: EU EUDAMED, US FDA

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EndoVive Initial Placement Standard PEG Kit with ENFit Connector, EndoVive Initial Placement Safety PEG Kit with ENFit Connector

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Oticon

FDA UDI
Oticon A/S·05707131281050·NERA2 PRO, MINIBTE 312 WL 85 DBL

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100561·GINSBERG EYE SPECULUM

HNM Women Care

FDA UDI
HNM STAINLESS, LLC.·00812171027737·PESSARY, CUBE #8, W/DRAINS, 63mm

CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·February 15, 2021

DEL MAR MONOAXIAL PEDICLE SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CUTERA SOLERA OPUS AESTHETIC PRODUCT

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

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code KWP·July 28, 2019

CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·May 27, 2024

WAVEWRITER ALPHA? 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 28, 2025

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

IVT DISPOSABLE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - THETFORD·Product code LHI·June 6, 2013

ACCURUS 400VS

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 22, 2011

CD HORIZON® SOLERA® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC MEDICAL COSTA RICA S.R.L.·Product code KWP·December 30, 2025

BD VACUTAINER® ADAPTER WITH LUER ADAPTER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 2, 2019

CD HORIZON® SOLERA® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC MEDICAL COSTA RICA S.R.L.·Product code KWP·June 10, 2025

TSRH® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC MEDICAL COSTA RICA S.R.L.·Product code NKB·January 22, 2026

BD SYRINGE LUER-LOK¿ TIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·March 7, 2018