91 results
·
27ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO ALPHA DX SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Tandem Mobi Autosoft XC Kit
FDA UDI
Tandem Diabetes Care, Inc.·00389152311876·Autosoft XC, 5"/6mm, 2 pack kit
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033457986·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0131100·Rod Inserter, Fixed, 90 Degree, MIS
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033457955·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033457993·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033457962·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021586435·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568628542·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0131100·Assembly, Rod Inserter, Fixed UNID
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033458006·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033457979·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131100·Rocker, One Piece
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568586439·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131150·Rocker, Hinged Locking
NORMED MANDIBULAR FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Z2 BALLOON GUIDED PACING & PRESSURE MONITORING CATHETER, MODEL Z2-7-02-1-10-0
FDA 510(k)
FDA Class 2
·Cardiovascular
8018514
FDA Adverse Event
Malfunction
·October 30, 2018
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 22, 2006
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 22, 2006