28 results · 32ms · Sources: EU EUDAMED, US FDA

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TempSure

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704293227·

Sklar®

FDA UDI
SKLAR CORPORATION·10649111140532·RANKIN KELLY FCP STR 6.25"

FLEXI-LITE

FDA 510(k)
FDA Class 2 ·Anesthesiology

ELECTROSURGICAL MONOPOLAR CABLE/ADAPTERS, ELECTROSURGICAL BIPOLAR CABLE/ ADAPTERS, BIPOLAR ELECTROSURGICAL CABLES, MONOP

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·April 4, 2022

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·February 22, 2022

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·February 2, 2022

VITALITY 2

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 21, 2011

PENUMBRA RUBY COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code KRD·June 14, 2013

UNKNOWN DEPUY PINNACLE METAL HEAD 36MM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·September 19, 2008

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

FDA Enforcement
Class II ·Terminated·Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical·June 12, 2019

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·November 23, 2022

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·Product code ITX·May 25, 2021

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·April 16, 2024

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Injury ·COOK VANDERGRIFT INC·Product code ITX·April 2, 2024

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Malfunction ·COOK VASCULAR INC·Product code ITX·September 5, 2018

COOK-SWARTZ DOPPLER PROBE

FDA Adverse Event
Malfunction ·COOK VANDERGRIFT INC·Product code ITX·October 31, 2023

OPEN-END FLEXI-TIP URETERAL CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KOD·February 6, 2020

OPEN-END URETERAL CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KOD·February 7, 2020