29 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION
FDA 510(k)
FDA Class 2
·Cardiovascular
Sasmar Vanilla
FDA UDI
Sasmar Pharmaceuticals SPRL·09337213008266·PERSONAL LUBRICANT
EVONOS
FDA UDI
Gyrus ACMI, LLC·00821925018594·MINI MC GEE SCISSORS
Plateau C
FDA UDI
Life Spine, Inc.·00190837093648·
Zavation
FDA UDI
Zavation LLC·00842166176621·Tower Removal Tool
5131044
FDA Adverse Event
Malfunction
·October 7, 2015
Zavation
FDA UDI
Zavation LLC·00842166176638·Tower Removal Tool
Zavation
FDA UDI
Zavation LLC·00842166176645·Push Rod
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L44mm
FDA UDI
Laboratoires Bodycad Inc·00688346002782·Button Head Locking HA 4.5 Cortical Self Tappin...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523106233·Porous Acetabular Cup System - Hemispherical Sh...
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166534·Initia T3 Acetabular Hemispherical Shell, Multi...
ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
FDA 510(k)
FDA Class 1
·Clinical Chemistry
RETRIEVE IMPLANT CEMENT
FDA 510(k)
FDA Class 2
·Dental
8110 ALARIS SYRINGE PUMP
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 24, 2020
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 28, 2025
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 3, 2024
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012