28 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VALLEYLAB E2750 LAPAROSCOPIC HANDSET, VALLEYLAB E2770 SERIES ELECTRODES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515251434·Freeman Flap Ret, 1" wide, 8"
SPONGE, SURGICAL, GAUZE, COMPRESSED 2 BY 2 INCHES
FDA 510(k)
FDA Unclassified
·Unknown
RAICHEM (TM) SPIA (TM) - ACID GLYCOPROTEIN REAGENT
FDA 510(k)
FDA Class 1
·Immunology
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2019
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 11, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 10, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 9, 2017
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·June 12, 2020
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 6, 2016
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 22, 2014
COMBI SET TRUE FLOW SERIES BLOOD TUBING -8MM PUMP
FDA Adverse Event
FRESENIUS MEDICAL CARE OF NORTH AMERICA·Product code FJK·February 8, 2013
TOTALCARE
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·December 21, 2010
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 7, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·July 22, 2016
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 12, 2018
TSRH
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 15, 2017
TSRH
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·May 14, 2017