14 results
·
27ms
·
Sources: EU EUDAMED, US FDA
IP-16
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79803011·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79803011001·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79803010101·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79803010051·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
AXIS 5.5 Lumbar Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
CAULK TYLOK
FDA 510(k)
FDA Class 2
·Dental
BD ANGIOCATH¿ IV CATHETER 22 G X 1"
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017
MAYFIELD INFINITY XR2 TRI-STAR SWIVEL ADAPTOR
FDA Adverse Event
Malfunction
·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·June 5, 2014
2520274-2013-10708
FDA Adverse Event
Malfunction
·SYNTHES (USA)·Product code MNI·February 22, 2013
PEG-24-PULL-S
FDA Adverse Event
Death
·COOK MEDICAL ,INC.·Product code KNT·January 25, 2011
Actiwatch 16 Part Number 198-0300-00, Actiwatch 16 AM 198-0300-AM; Actiwatch 64 Part Number 198-0301-00; Actiwatch 64 AM Part Number 198-0301-AM, Mini Mitter, a Respironics Company, Bend, Oregon
FDA Recall
Terminated
·Mini-Mitter Company, Inc.·Product code M·June 27, 2007
BD ANGIOCATH¿ IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017
Actiwatch 64 AM, Bandless Part Number 198-0301-AM1, Respironics, Inc., Mini Mitter, a Respironics Company, Bend, Oregon
FDA Recall
Terminated
·Mini-Mitter Company, Inc.·Product code M·June 27, 2007