25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOSCREW XTRALOK
FDA 510(k)
FDA Class 2
·Orthopedic
Medline Industries, Inc.
FDA UDI
MEDLINE INDUSTRIES, INC.·10884389000762·CIRCUIT-ADULT ANESTHESIA
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756135962·Airway Circuit
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021441604·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021441345·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021441376·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00887661650276·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021441352·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021441369·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0131300·Rod Inserter, Articulating, MIS
MODIFICATION TO: RADIOLUCENT COLLES FRACTURE KIT
FDA 510(k)
FDA Class 2
·Orthopedic
PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INFINITI VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 7, 2014
INFINITI VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 7, 2014
ENDOPATH ETS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 7, 1997
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
INFINITI VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 7, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·March 1, 2013
ASR ACETABULAR IMPLANT 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011