343 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LIDCO CNAP MODULE
FDA 510(k)
FDA Class 2
·Cardiovascular
Sasmar Vanilla
FDA UDI
Sasmar Pharmaceuticals SPRL·09337213008266·PERSONAL LUBRICANT
Zavation
FDA UDI
Zavation LLC·00842166176744·Dilator 3
Zavation
FDA UDI
Zavation LLC·00842166176737·Dilator 2
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L48mm
FDA UDI
Laboratoires Bodycad Inc·00688346002805·Button Head Locking HA 4.5 Cortical Self Tappin...
Zavation
FDA UDI
Zavation LLC·00842166176720·Dilator 1
5131048
FDA Adverse Event
Injury
·October 7, 2015
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523106257·Porous Acetabular Cup System - Hemispherical Sh...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166558·Initia T3 Acetabular Hemispherical Shell, Multi...
SYNTHES SCOUT TACK FIXATION
FDA 510(k)
FDA Class 2
·Cardiovascular
CARESTART HCG COMBO ONE-STEP PREGNANCY TEST AND CARESTART PLUS HCG COMBO ONE-STEP PREGNANCY TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021