39 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VU APOD INTERVERTEBRAL BODY FUSION DEVICE
FDA 510(k)
FDA Class 2
·Orthopedic
Aequalis™ Adjustable Reversed
FDA UDI
TORNIER, INC.·00846832068111·
ILIZAROV SYSTEMS
FDA UDI
MEDICALPLASTIC SRL·08033201841280·HALF RING INTERNAL DIAMETER 240MM SS
PAR/PAK II
FDA UDI
Bio/Data Corporation·G0561013101·
Tasso+
FDA UDI
Tasso Inc.·00850038691004·
Intuit Glide Transducer Cover
FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436111345·Sterile (14 × 91.5cm) accordian-folded CIV-Flex...
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0113100·Decorticating Planer
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780375043·Integra® Jarit® Strabismus Scissors, 4-1/2", Ca...
NIEN MADE NON-INVASIVE BLOOD PRESSURE MONITOR, MODELS HP-BPM0001; HP-BPM0002; HP-BPM0003; HP-BPM0003-1
FDA 510(k)
FDA Class 2
·Cardiovascular
VITROS CHEMISTRY PRODUCTS CREA SLIDE, VIRTROS CHEMISTRY PRODUCTS CALIBRATOR KIT 1
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Specials
FDA UDI
Seaspine Orthopedics Corporation·10889981308261·Rotary Scraper/Dilator, 10mm w/ Depth Grooves
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 8, 2025
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·July 16, 2020
ADVANIX BILIARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 5, 2024
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019
GMK-PRIMARY FEMUR PS CEMENTED SIZE 4 LEFT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·August 23, 2017
GMK-PRIMARY FEMUR PS CEMENTED SIZE 6 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 25, 2018
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code LOX·December 16, 2022
ADVANIX BILIARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 30, 2024
TREK¿
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code LOX·May 27, 2025