24 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PATHFINDER SYSTEM POLYAXIAL PEDICLE SCREWS

FDA 510(k)
FDA Class 2 ·Orthopedic

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496071174·STRIPE GAME ANDROMEDA, SIZE M, NERO, GRADUATED ...

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292886·

Key Surgical K-Wires and Steinmann Pins

FDA UDI
KEY SURGICAL, INC.·00849771012610·K-Wires, Single trocar, .054-inch (1.4mm) diame...

NA

FDA UDI
KEY SURGICAL, INC.·10849771049200·K-Wires, Single trocar, .054-inch (1.4mm) diame...

K-Wire w. trocar/round end 1.37mm/127mm, 6 pcs./unit

FDA UDI
mahe medical gmbh·EMAHKM711740·K-Wire w. trocar/round end 1.37mm...

mahe medical GmbH

FDA UDI
mahe medical gmbh·04050659484429·K-Wire w. trocar/round end _x000D_...

CONMED

FDA UDI
Conmed Corporation·10845854006344·OSCILLATOR BLADE, 19.5 X 86 X 0.8 MM (.031")

NA

FDA UDI
STERILMED, INC.·10888551020510·SAW BLADE OSCILLATING LARGE BONE

Up & Up

FDA UDI
TARGET CORPORATION·00845717009362·Up&Up Heat Wrap - Back/Large Areas, 3 count

Up&Up

FDA UDI
TARGET CORPORATION·06945397903340·Heat Wraps for Low Back + Hips - 3ct - Up&Up

Up&Up

FDA UDI
TARGET CORPORATION·06945397906167·Heat Wraps for Low Back + Hips - 3ct - Up&Up

COSMED QUARK

FDA 510(k)
FDA Class 2 ·Anesthesiology

PARADIGM-FONTONA PEROVSKITE ND: YAP LASER SYSTEM AND ACCESSORIES

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

LINEAR 3-6

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 6, 2022

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 8, 2021

SPECTRA WAVEWRITER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 3, 2020

DEPUY ASR XL FEM IMP SIZE 47

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·April 22, 2013

SPRINT FIDELIS

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 27, 2011

2500

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 10, 2008