26 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RADIOACTIVE SEEDS
FDA 510(k)
FDA Class 2
·Radiology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902391286·INSTRUMENT 8910710 INSERTER LG PEEK VS
ZAVATION
FDA UDI
Zavation LLC·00842166151840·WHITNEY 13mmx15mm , 7deg , 10mm
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756372954·REGULAR INJECTIONS PACK
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112250·SURG-I-BAND YELLOW
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN
TiWAVE L Lumbar Cage System
FDA UDI
Kalitec Direct LLC·B07323K0107100·Tamp, Rotating
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345023796·Angled Tamp
EliA SymphonyS Immunoassay
FDA 510(k)
FDA Class 2
·Immunology
SEEDLING ENTERPRISES LLC, COOL TEC MONOPOLAR AND BIPOLAR REUSABLE ELECTRODES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·December 4, 2012
NITINOL GUIDEWIRE WI/FLOPPY PLATINUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code DYB·November 30, 2010
ESSURE
FDA Adverse Event
Injury
·BAYER·Product code HHS·July 2, 2014
COMPREHENSIVE REVERSE HUMERAL TRAY 44MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·March 17, 2017
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 18, 2020
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 23, 2020
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021