17 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFIED C.P.R. MICROSHIELD
FDA 510(k)
FDA Class 1
·Anesthesiology
SW
FDA UDI
SW SAFETY SOLUTIONS INC.·00616489125532·PowerChem Neoprene Exam Gloves, Medium
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR78714031·Mini Sprint Bracket Roth .018" mand. 3 left w. ...
LinkBio Instrument
FDA UDI
Link Bio Corp·00810022403044·Fusion Nail Femoral Trial Left
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR78714030101·Mini Sprint Bracket Roth .018" mand. 3 left w. ...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR78714030051·Mini Sprint Bracket Roth .018" mand. 3 left w. ...
Mini-Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR78714031001·Mini Sprint Bracket Roth .018" mand. 3 left w. ...
OralTox Oral Fluid Drug Test
FDA 510(k)
FDA Class 2
·Clinical Toxicology
X3C 1600 DIGITAL RADIOGRAPHIC SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 28, 2015
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 12, 2012
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·October 15, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 29, 2014
SPARC SLING SYSTEM
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·December 5, 2012
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 26, 2013
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024
Alcon Custom Pak
FDA Enforcement
Class II
·Ongoing·Alcon Research, LTD.·August 23, 2023