6,648 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FemChec
FDA UDI
FEMASYS INC.·00859500005097·FemChec Controlled Saline-Air Device, FCD-250 B...
Demo Flight case
FDA UDI
PLASMABIOTICS·03701354404908·Demo Flight case
PENTAX CHOLEDOCHOFIBERSCOPE, #FCD-15A
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
4.5mm Drill Bit
FDA UDI
SURGENTEC, LLC·00858406007495·
PERPOS FCD-2 System
FDA UDI
INTERVENTIONAL SPINE, INC·81195401018862·PERPOS FCD-2 Anchor, 4.5mm Diameter by 28-35mm ...
PERPOS FCD-2 System
FDA UDI
INTERVENTIONAL SPINE, INC·81195401011900·Instruments with Teleport and Tray
FCD-2 IMPLANT SYSTEM
FDA UDI
DECIMA SPINE, INC.·00857360007190·FCD-2 Implant System, ANCHOR
PERPOS FCD-2 System
FDA UDI
INTERVENTIONAL SPINE, INC·81195401019548·PERPOS FCD-2 Anchor, 4.5mm Diameter by 37-44mm ...
FCD-2 IMPLANT SYSTEM
FDA UDI
DECIMA SPINE, INC.·00857360007176·FCD-2 Implant System, Stabilizer
PERPOS FCD-2 System
FDA UDI
INTERVENTIONAL SPINE, INC·81195401020124·PERPOS FCD-2 Stabilizer, 4.5mm I. D. x 10mm O. D.
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094307092·Surveyor S19 GEN2 Patient Monitoring System - S...
FemChec Controlled Saline-Air Device (FCD-250)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PERPOS FCD-2 Removal Kit
FDA UDI
INTERVENTIONAL SPINE, INC·81195401050824·1 Stabilizer Removal Tool, 1 Anchor Removal Too...
Perpos FCD-2, Cassette Assembly
FDA UDI
INTERVENTIONAL SPINE, INC·81195401208324·Instruments Tray
BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·C. R. BARD, INC.·Product code KNT·January 30, 2025
UNKNOWN FECAL MANAGEMENT (DIGNISHIELD)
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code KNT·March 23, 2026
MEDTRONIC NAVIGATION
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC·Product code HAW·October 1, 2021
UNKNOWN FECAL MANAGEMENT (DIGNISHIELD)
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code KNT·March 23, 2026
BARD® DIGNISHIELD® STOOL MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·C.R. BARD INC.·Product code KNT·March 15, 2018
PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER
FDA 510(k)
FDA Unclassified
·Unknown