22 results · 20ms · Sources: EU EUDAMED, US FDA

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Sheath Introducer

FDA 510(k)
FDA Class 2 ·Cardiovascular

ZEUS-O

FDA UDI
SPINAL ELEMENTS·00840916122492·Zeus-O Implant, 15 x 09 x 32mm

Leg Bag

FDA UDI
C. R. Bard, Inc.·00801741050909·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...

Oticon

FDA UDI
Oticon A/S·05707131280398·RIA2 PRO TI, BTE 13 WL 85 CBE DEMO

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587P1509320·15mm PLIF Implant 9mm Wide 32mm Length

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587P15093270·15mm PLIF Implant 9mm Wide 32mm Length 7 Degrees

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869607704·TELIX K Ti Cage 9x32mm 5°

INCLUSIVE MINI IMPLANT

FDA 510(k)
FDA Class 2 ·Dental

DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

RADIFOCUS OPTITORQUE

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2013

ACCU-CHEK AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 3, 2008

AUGMENTED INSERT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 29, 2011

MREYE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018

MREYE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018

MREYE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018

NESTER PLATINUM EMBOLIZATION MICROCOIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018

MREYE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018

BD VACUTAINER® 9NC 0.109M PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 6, 2018

MREYE EMBOLIZATION COIL

FDA Adverse Event
Injury ·COOK INC·Product code KRD·May 11, 2018