117 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HL168E
FDA 510(k)
FDA Class 2
·Cardiovascular
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00141221·
CoverLoc™ Volar Plate
FDA UDI
TORNIER, INC.·00846832001439·FULLY THREADED SCREW
Tandem Mobi TruSteel Kit
FDA UDI
Tandem Diabetes Care, Inc.·00389152412276·TruSteel, 23"/6mm, 10 pack kit
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563892·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563908·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563915·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563922·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563878·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563861·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033563885·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142120·Trial, TLIF, 32L OB CRV 7Deg, 12mm
BALLPEN SPINAL NEEDLE W/WO INTRODUCER
FDA 510(k)
FDA Class 2
·Anesthesiology
CONTINUOUS FLOW Y-TUBING
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·October 4, 2018
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
QUICKSITE LV
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·March 10, 2011
ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code HQL·March 13, 2008
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026
BD BACTEC¿ MGIT¿ 960 SIRE KIT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·March 26, 2026