34 results
·
20ms
·
Sources: EU EUDAMED, US FDA
NEW EYES EYEGLASS FRAME
FDA 510(k)
FDA Class 1
·Ophthalmic
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074052304·SPREADER 2940250 CAM 6MM
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780415138·Integra® Miltex® Tissue Nipper, 4-1/2", Convex ...
VARIAX
FDA UDI
Stryker GmbH·07613327125627·Reduction Instrument Insert 1
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199656·Modular Knee Stem Pilot 25mm x 100mm
N/A
FDA UDI
Tyber Medical, LLC·M695M9402500·
SBH
FDA UDI
SBH Surgical·00860011953494·Sterile Single Use Tissue Nail Nipper, 4.5"/11cm
3M STERI-DRAPE CHG ANTIMICROBIAL INCISE DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BONE-LOK HP WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 1, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 27, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 18, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 21, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 18, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 23, 2026
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 22, 2026
BD VACUTAINER® SERUM
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·December 10, 2025
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·May 5, 2026
ALARIS PC UNIT
FDA Adverse Event
Malfunction
·CAREFUSION CORPORATION·Product code FRN·April 7, 2014
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·February 2, 2013