21 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.

VIAL-MATE Adaptor

FDA 510(k)
FDA Class 2 ·General Hospital

McPHERSON CORNEAL TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896073500·McPHERSON CORNEAL TISSUE FORCEPS WITH TYING PLA...

Innomed, Inc.

FDA UDI
INNOMED, INC.·00840277101235·Cheng Screw Removal & Bone Trephine Set with Case

UNKNOWN COOLSCULPTING SYSTEM

FDA Adverse Event
Injury ·ALLERGAN PLEASANTON·Product code OOK·July 12, 2021

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04059993057467·ELVAREX FORTE 3/CHAP STYLE/PROFILE-SLANT-CLOSED...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702563177·ELVAREX 2/KNEE HIGH/PROFILE-SLANT-CLOSED TOE/DO...

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702253825·ELVAREX 2/THIGH HIGH/SLANT, CLOSED TOE, KNEE FU...

ZAVATION

FDA UDI
Zavation LLC·00842166186637·14mm X 26mm 0° Trial

BK-1426-00-01 STONYBROOK/HI-WALL PLATE

FDA 510(k)
FDA Class 1 ·Physical Medicine

UniTip Catheter

FDA UDI
Unisensor AG·07640172971369·

UniTip Catheter

FDA UDI
Unisensor AG·07640172973233·

STANSION MATRIX

FDA 510(k)
FDA Class 2 ·Orthopedic

SIMPLYGO BREAST PUMP

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

LIFEPAK(R) 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

LIFEPAK® 1000 DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FPA·June 3, 2013

DUROM ACETABULAR COMPONENT

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code LZO·September 30, 2014

DAILY ACTIVITY ASSIST DEVICES

FDA Adverse Event
Malfunction ·PINGHU WEIFENG MATERIAL TECHNOLOGY·Product code IKX·June 21, 2011

PROLENE BLUE 1.50M 45CM W/NDL

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·June 2, 2022

ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,

FDA Enforcement
Class III ·Terminated·Ameditech Inc·December 30, 2015