28 results
·
27ms
·
Sources: EU EUDAMED, US FDA
FACTOR X DEFICIENT PLASMA
FDA 510(k)
FDA Class 2
·Hematology
ReLine
FDA UDI
Nuvasive, Inc.·00195377068347·RELINE C Screw, 4.5x10mm Occipital
CoRoent
FDA UDI
Nuvasive, Inc.·00887517385567·CoRoent XL Trial, 10x18x55mm
SOMATEX
FDA UDI
BIOPSYBELL SRL·08033860021733·
Mariner
FDA UDI
Seaspine Orthopedics Corporation·10889981129057·Head Turner
microTargeting™ Insertion Tube Set
FDA UDI
FHC, INC.·00873263004104·microTargeting Single Electrode Insertion Tube ...
SYNCHRON SYSTEMS ALCOHOL REAGENT AND CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
COOLTOUCH THERMAL SENSING HANDPIECE ACCESSORY
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Intervertebral Body Fusion Device
FDA UDI
PRECISION SPINE, INC.·00840019923521·PLIF Sizer 10mm x 22mm
CURE LP
FDA UDI
SpineArt SA·07640332475270·FIXED DRILL GUIDE
TCP
FDA UDI
WRIGHT MEDICAL TECHNOLOGY, INC.·00840420118912·
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 3/11 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·November 18, 2019
PHYSICA KR FEMUR COMP.RIGHT #6
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code HRY·October 21, 2022
UNKNOWN PALACOS CEMENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KRO·April 12, 2017
OEC
FDA UDI
TIDI PRODUCTS, LLC·00618125152193·Gray Footswitch Cover All OEC Systems Box of 25
FOLFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 27, 2014
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 7, 2013
STENOSCOPE
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·October 26, 2010
Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only, UDI:00886874115978
FDA Enforcement
Class II
·Terminated·Intuitive Surgical, Inc.·October 20, 2021
FEMORAL MODULAR HEAD - M Ø32MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·August 26, 2021