33 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01
FDA 510(k)
FDA Class 2
·Neurology
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994325563·CONNECTOR 7022420 LAT CONN SS 6.35 22MM
GALILEO® TROCHANTERIC NAIL, LEFT, Ø11mm x 42cm x 125°
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665014402·
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113690·PS-C Insert, Size 4 x 20mm
Mariner Outrigger
FDA UDI
Seaspine Orthopedics Corporation·10889981173760·Closed, Axial Rod, Long, 420mm
HITACHI ALTAIRE
FDA 510(k)
FDA Class 2
·Radiology
PARACON II/FECAL CONCENTRATOR II
FDA 510(k)
FDA Class 1
·Microbiology
CADD-SOLIS VIP AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FRN·May 1, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 8, 2026
ABG SYRINGE,1 ML LUER-LOK SYRINGE WITH NEEDLE. REGULAR PLUNGER STOPPER &TIP CAP.
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017
BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 6, 2017
3 ML BD PRESET¿ SYRINGE WITH BD LUER-LOK¿ TIP. 22 G X 1 IN BD ECLIPSE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 4, 2017
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 7, 2018
35MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·September 24, 2025
35MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·January 14, 2025
BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 27, 2017
BD PRESET¿ SYRINGE WITH ATTACHED NEEDLE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 7, 2017
25MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·September 24, 2025
25MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·June 20, 2025
35MM TAP
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code LXH·March 21, 2025