39 results · 20ms · Sources: EU EUDAMED, US FDA

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VOLU-SOL HISTO./CYTO. STAIN MOD. #EA65

FDA 510(k)
FDA Class 1 ·Hematology

Elite Orthopaedics

FDA UDI
Elite Orthopaedics, Inc.·00816591013387·Post Op Telescoping Knee Brace

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306810077·Blunt Injector, 18G x 7cm, Luer

Elite Orthopaedics

FDA UDI
Elite Orthopaedics, Inc.·00816591013998·OA Knee Brace, Single Upright, Right

Elite Orthopaedics

FDA UDI
Elite Orthopaedics, Inc.·00816591014001·OA Knee Brace, Single Upright, Left

Falcon

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730088604·Bird Beak Pliers w/Cutter

PERI-LOC LOCKING HOLE INSERTS AND CABLE ACCESSORIES

FDA 510(k)
FDA Class 2 ·Orthopedic

IGROK

FDA 510(k)
FDA Class 2 ·Radiology

PROLENE POLYPROPYLENE SUTURE

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code GAW·May 8, 1998

PLATE CDC ANAEROBE 5% SB 100 EA JP

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·September 9, 2021

PLATE CDC ANAEROBE 5% SB 20 EA

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JSG·June 28, 2021

BIODESIGN URETHRAL SLING

FDA Adverse Event
Injury ·COOK BIOTECH, INC.·Product code PAG·April 3, 2014

TRANSTAR STRETCHER

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FPO·October 9, 2012

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 28, 2007

SMR HUMERAL HEAD Ø48 MM

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code KWT·May 8, 2024

SMR REVERSE FINNED HUMERAL BODY

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code PHX·September 29, 2023

PLATE CDC ANAEROBE AGAR 5% SB 90MM 20

FDA Adverse Event
Malfunction ·BECTON DICKINSON GMBH·Product code JSG·February 17, 2022

SMR CEMENTLESS FINNED STEM

FDA Adverse Event
Injury ·LIMACORPORATE SPA·Product code HSD·September 13, 2019

Optiflux F180NR Dialyzers, Catalog Number: 0500318E. Manufactured by Fresenius Medical Care North America, Ogden, UT 84404. Designed for single use acute and chronic hemodialysis.

FDA Recall
Terminated ·Fresenius Medical Care North America·Product code KDI·May 14, 2010

Trinity Biotech, Captia VZV IgG. Product code 2325600: 96 Tests; product code: 2325601: 480 tests. For in vitro diagnostic use. Intended for the detection and quantitative determination of IgG antibody to VZV in human sera.

FDA Recall
Terminated ·Clark Laboratories, Inc. (dba, Trinity Biotech USA)·Product code GQX·May 29, 2012