43 results
·
22ms
·
Sources: EU EUDAMED, US FDA
NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450430224·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033461990·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033461983·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462010·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033461969·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033462003·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033461976·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0131300·Rod Inserter, Articulating, MIS
MULTIPLE-VINYL EXAM GLOVE, POWDERED
FDA 510(k)
FDA Class 1
·General Hospital
VERSALUX
FDA 510(k)
FDA Class 2
·Dental
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·August 13, 2018
IMMULITE 2000 3GALLERGY SPECIFIC IGE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018
IMMULITE 2000 3GALLERGY SPECIFIC IGE
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED·Product code DHB·May 22, 2018
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·March 1, 2013
ASR ACETABULAR IMPLANT 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·August 15, 2014
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code MJO·April 24, 2014
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·June 19, 2014
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·June 25, 2014