26 results · 23ms · Sources: EU EUDAMED, US FDA

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CELL-DYN 1800 SYSTEM

FDA 510(k)
FDA Class 2 ·Hematology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526827851·***DISC*LEVAMED ANKLE SUPPORT BLACK III

Latitude™ EV

FDA UDI
TORNIER, INC.·00846832002887·Humeral Stem - Coated

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482043707·Symmetry® Scissors, Operating, Curved, Sharp/Sh...

NA

FDA UDI
STRYKER CORPORATION·07613153001423·5.0mm Round Solid Carbide Bur Extra Long

TAXOL ADMINISTRATION SET

FDA 510(k)
FDA Class 2 ·General Hospital

MODIFICATION TO EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

21GX.75IN. BD VACUTAINER® WINGED SAFETY PBBCS WITH 12 IN TUBING

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 27, 2017

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·February 5, 2024

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET PRE-ATTACHED HOLDER 23G NEEDLE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 3, 2017

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·January 31, 2024

ASR UNI FEMORAL IMPL SIZE 45

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 2, 2013

FIRST PICC KIT W/ INTROSYTE-N INTRODUCER

FDA Adverse Event
Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code LJS·March 22, 2011

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·April 16, 2008

LOGIC TIB INSERT IMPL CRC, SZ 4, 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 3, 2023

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 3, 2024

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·February 28, 2024

Stryker Locking Screw, Fully Threaded T2 Tibia ¿5x35 mm Catalog Number: 18965035S - Product Usage: Stryker implants are single use devices intended for the temporary fixation, correction or stabilization of bones.

FDA Enforcement
Class II ·Terminated·Stryker GmbH·June 24, 2020

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·January 18, 2024

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·December 14, 2023