16 results
·
28ms
·
Sources: EU EUDAMED, US FDA
INSUFLOW SYNERGY XL PORT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772814671·GENUMEDI SILVER SIZE IV
Peerless Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989053586·PEERLESS 2NDMOL 6DEG LR NDX-20TX018
NexxZr™ T / D-100-20-NT-OM30-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271114143·
MODIFICATION TO VASCULAR SOLUTIONS VARI-LASE ENDOVENOUS LASER PROCEDURE KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SYRINGE 0.3ML 31GA 8MM
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·June 23, 2021
SYRINGE 0.3ML 31GA 8MM 10BAG 500 WAL
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·February 3, 2021
BD INSULIN SYRINGE 3/10ML 29G X 8MM
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·April 26, 2021
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·UNKNOWN·Product code CAW·October 1, 2014
TROCHANTERIC NAIL KIT, TI GAMMA3 Ø10X170MM X 125°
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·May 29, 2013
CLARION
FDA Adverse Event
Injury
·ADVANCED BIONICS LLC·Product code MCM·June 13, 2011
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·February 3, 2017
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·March 10, 2017
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code HBC·March 26, 2018
BBL Brain Heart Infusion Agar w/10% Sheep Blood - Catalog Number 297655.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004