17 results · 27ms · Sources: EU EUDAMED, US FDA

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INORGANIC PHOSPHORUS REAGENT SET

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

FIXATE TISSUE BAND

FDA 510(k)
FDA Class 2 ·Neurology

SYNERGY FLOW

FDA 510(k)
FDA Class 2 ·Dental

UniTip Catheter

FDA UDI
Unisensor AG·07640172972113·

UniTip Catheter

FDA UDI
Unisensor AG·07640172971604·

UniTip Catheter

FDA UDI
Unisensor AG·07640172971611·

UniTip Catheter

FDA UDI
Unisensor AG·07640172973585·

UniTip Catheter

FDA UDI
Unisensor AG·07640172972106·

M2A-38 CUP NON FLARED SZ 60MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014

PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC MILACA, INC.·Product code LWP·October 31, 2012

RSVR MMT-332A 10PK PRDGM 3CC 14L

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FMF·August 20, 2010

OXF ANAT BRG LT MD SIZE 4 PMA

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·September 28, 2022

OXF UNI TIB TRAY SZ B LM PMA

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code NRA·September 28, 2022

8015 ALARIS SYSTEM PC UNIT

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 21, 2020

ORTHOPEDIC SALVAGE SYSTEM COMPRESS SEGMENTAL FEMORAL COMPONENT LEFT 8.5CM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·March 4, 2019

CPS XS SHT SPDL W PINS 600LBF

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 23, 2019

CPS CENTERING SLEEVE 21MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 23, 2019