9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 1.4MM, SURELOCK ALL-SUTURE ANCHOR WITH INSERTER, 2.2MM
FDA 510(k)
FDA Class 2
·Orthopedic
STAR (LUNAR SERIES) MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
IROOT FS
FDA 510(k)
FDA Class 2
·Dental
GMK-PRIMARY TIBIAL INSERT UC FIXED SIZE 2 / 14 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 4, 2019
UNKN COBLATION ENT DEV
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·August 15, 2021
UNKN COBLATION ENT DEV
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·August 15, 2021
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 29, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·October 1, 2014