39 results · 24ms · Sources: EU EUDAMED, 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