16 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IODOFLEX PASTE
FDA 510(k)
FDA Class 1
·General Hospital
AXSOS
FDA UDI
Stryker GmbH·07613327085976·Instrument Insert Titanium 4.0mm ORIF
IMBIBE NEEDLE
FDA 510(k)
FDA Class 1
·Orthopedic
COLOR OPTIC CORNEAL EYE SHIELD
FDA 510(k)
FDA Class 1
·Ophthalmic
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 20, 2026
MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN·Product code BTR·June 18, 2014
BIPOLAR LEAD ADAPTER
FDA Adverse Event
Injury
·GREATBATCH MEDICAL·Product code DTB·December 20, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code NKB·February 3, 2013
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Injury
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 18, 2026
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 27, 2026
OPERATING CYSTOSCOPE-URETHROSCOPE
FDA Adverse Event
Death
·KARL STORZ SE & CO. KG·Product code FGB·March 8, 2023
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Injury
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 18, 2026
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·March 20, 2024
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·October 26, 2023
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·November 20, 2023
Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.
FDA Enforcement
Class II
·Terminated·Capintec Inc·April 1, 2020