12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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THUNDERBEAT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ThermoCool SmartTouch
FDA UDI
Biosense Webster Inc·10846835009187·
Healthweigh
FDA UDI
Rice Lake Weighing Systems, Inc.·00850042373484·Scale,RL-MPS-30 180kg x 100g including metric h...
Innomed, Inc.
FDA UDI
INNOMED, INC.·00840277100948·Cannestra Hip Length Gauge Ruler
INNOVATECH STRAIGHT LASER PROBE, MODEL 420-10
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BUILD-IT TOTAL CORE
FDA 510(k)
FDA Class 2
·Dental
AMISTEM H FEMORAL CEMENTLESS STEM SIZE 1 STD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·February 27, 2014
ThermoCool SmartTouch Navigation Catheters, Catalog No. D132701, D132702, D132703, D132704, D132705, D133601, D133602, D133603.
FDA Enforcement
Class II
·Terminated·Biosense Webster, Inc.·November 5, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·May 29, 2013
ADVANCE BED
FDA Adverse Event
HILL-ROM INC.·Product code FNL·June 10, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Death
·CORDIS DE MEXICO·Product code NIQ·August 22, 2008
ThermoCool SmartTouch Navigation Catheters, Catalog No. D132701, D132702, D132703, D132704, D132705, D133601, D133602, D133603.
FDA Recall
Terminated
·Biosense Webster, Inc.·Product code LPB·October 19, 2014