80 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REPEL SURGICAL GLOVE LINERS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Instruments
FDA UDI
Nuvasive, Inc.·00887517385147·ALGI Curette, Straight Medium
Tibial Spacer
FDA UDI
ADLER ORTHO SPA·08052693620555·10 mm LB TIBIAL SPACER
Peerless Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989022650·ASSY ORTHOS A/P SGL -4LFM -10X18 LR
Mariner
FDA UDI
Seaspine Orthopedics Corporation·10889981129484·Set Screw Starter, 1/4 sq
TOTALSHIELD®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024376441·Zippered Surgical Toga, Regular
Intervertebral Body Fusion Device
FDA UDI
PRECISION SPINE, INC.·00840019923309·TLIF Sizer 10mm x 24mm
VOYAGER 6.0 SOFTWARE OPTION
FDA 510(k)
FDA Class 2
·Neurology
EQUIVABONE
FDA 510(k)
FDA Class 2
·Orthopedic
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DRA·June 11, 2025
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code DRA·October 3, 2025
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DRA·August 27, 2025
FLEXCATH CROSS TRANSSEPTAL SOLUTION
FDA Adverse Event
Injury
·ACUTUS MEDICAL INC·Product code DYB·November 4, 2025
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code DRA·December 10, 2024
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code DRA·December 10, 2024
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 27, 2014
SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 7, 2013
CELL-DYN EMERALD DILUENT
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·November 16, 2010
PULSESELECT
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code QZI·March 23, 2026
FLEXCATH CONTOUR¿ STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRA·March 23, 2026