40 results
·
32ms
·
Sources: EU EUDAMED, US FDA
SYNGO DYNAMICS, VERSION 9.0
FDA 510(k)
FDA Class 2
·Radiology
AOS Trocar Tip Guide Wire, 2.0mm x 150mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665000054·
Clear Readers
FDA UDI
Diversified Products, Inc.·00842894121702·
SAV
FDA UDI
Diversified Products, Inc.·00037741210221·
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112861·CORNEAL TREPHINE BLADE6.0MM
Orthopaedic Surgical Instruments
FDA UDI
CITIEFFE SRL·08056711921211·
Clear Readers
FDA UDI
Diversified Products, Inc.·00842894113554·
SAV
FDA UDI
Diversified Products, Inc.·00842894114254·
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800039825917·Rod 5.5 x 150mm
SONICAID FM820, SONICAID FM830
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PATTON ENDO-BAG
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
REPICCI TIBIAL 37X6.5MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HRY·April 20, 2015
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 19, 2022
M2A-MAGNUM PF CUP 56ODX50ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·September 18, 2018
RECAP CMT FMRL HD RESUR 50M
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KXA·September 18, 2018
M2A-MAGNUM PF CUP 56ODX50ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·September 18, 2018
RECAP CMT FMRL HD RESUR 50M
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KXA·September 18, 2018
PALACOS R 1X40 SINGLE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LOD·April 15, 2019
TRUEMETRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH, INC.·Product code NBW·December 13, 2016
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 3, 2013