26 results · 28ms · Sources: EU EUDAMED, US FDA

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RADIOACTIVE SEEDS

FDA 510(k)
FDA Class 2 ·Radiology

N/A

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902391286·INSTRUMENT 8910710 INSERTER LG PEEK VS

ZAVATION

FDA UDI
Zavation LLC·00842166151840·WHITNEY 13mmx15mm , 7deg , 10mm

DeRoyal

FDA UDI
DEROYAL INDUSTRIES, INC.·00749756372954·REGULAR INJECTIONS PACK

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668112250·SURG-I-BAND YELLOW

Gen. Acces/ Instr. Tip Guard

FDA UDI
KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN

TiWAVE L Lumbar Cage System

FDA UDI
Kalitec Direct LLC·B07323K0107100·Tamp, Rotating

neoWave LS

FDA UDI
XENIX MEDICAL LLC·00818345023796·Angled Tamp

EliA SymphonyS Immunoassay

FDA 510(k)
FDA Class 2 ·Immunology

SEEDLING ENTERPRISES LLC, COOL TEC MONOPOLAR AND BIPOLAR REUSABLE ELECTRODES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

TOTALCARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·December 4, 2012

NITINOL GUIDEWIRE WI/FLOPPY PLATINUM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code DYB·November 30, 2010

ESSURE

FDA Adverse Event
Injury ·BAYER·Product code HHS·July 2, 2014

COMPREHENSIVE REVERSE HUMERAL TRAY 44MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·March 17, 2017

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 18, 2020

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·October 23, 2020

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·November 28, 2020

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 20, 2021

PENTAX

FDA Adverse Event
Injury ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 18, 2021