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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