31 results · 26ms · 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.

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814695·GENUMEDI SILVER SIZE VI

ELI 10 ELECTROCARDIOGRAPH MODEL ELI 10

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814640·GENUMEDI SILVER SIZE I

REPICCI II RESURFACING KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304447110·

DURAVENT

FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948005448·DURAVENT UNI 1 IC + 1 ICU, SIZE 6

Plateau Spacer System

FDA UDI
Life Spine, Inc.·00190837026035·PLATEAU Interbody, Straight, Bulleted, 10mm 22m...

ALTERNANAS PROCESSING SYSTEM, CH 2000 CARDIAC DIAGNOSTIC SYSTEM, HEARTWAVE ALTERNANS PROCESSING SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

HI-TORQUE WHISPER LS GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER MS GUIDE WIRE WITH HYDROCOAT HYDRO

FDA 510(k)
FDA Class 2 ·Cardiovascular

TGS UKA SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC·Product code HSX·March 22, 2013

EPIPHANY

FDA UDI
PANTHEON SPINAL, LLC·B528100204041022060·#4 15 DEGREE CURVED DOWN CURETTE SHAFT

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·May 6, 2013

TGS UKA SYSTEM

FDA Adverse Event
Injury ·CAYENNE MEDICAL, INC·Product code HSX·February 12, 2014

TGS UKA SYSTEM

FDA Adverse Event
Injury ·CAYENNE MEDICAL, INC.·Product code HSX·September 25, 2014

INFUSE BONE GRAFT 12 MG

FDA Adverse Event
Injury ·MEDTRONIC·Product code NEK·May 1, 2014

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·September 10, 2013

TGS UKA KNEE SYSTEM

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, LLC·Product code HSX·August 14, 2013

32MM I.D. 7MM OFFSET SIZE HH LINER USE WITH 50MM O.D. SIZE HH SHELL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 31, 2023

METRX

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code LXH·May 9, 2013

MELODY TRANSCATHER PULMONARY

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·September 19, 2014

7900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 19, 2011