23 results · 24ms · Sources: EU EUDAMED, US FDA

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MVP Cervical Plate System

FDA 510(k)
FDA Class 2 ·Orthopedic

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776165208·Volkman Retractor , prongs sharp, ring handle

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780181965·Integra® Jarit® Volkman Retractor, 4-5/8", 2 Pr...

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306804151·Tyrell ( Iris ) Skin Hook, Delicate, Round Hand...

Ophthalmic Retractor

FDA UDI
KATENA PRODUCTS, INC.·00841668101087·HELVESTON "BARBIE" RETRACTOR

SPYSCOPE ACCESS AND DELIVERY CATHETER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

RAPTOR FACET FIXATION SYSTEM

FDA 510(k)
FDA Unclassified ·Unknown

FASTTAKE

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code NBW·July 11, 2005

OT VERIO2 METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 14, 2018

OT VERIO FLEX METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·April 4, 2019

GALAXY G3 MINI 2MM X 3CM

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·May 20, 2020

OT VERIO2 METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 20, 2016

MONACO

FDA Adverse Event
Malfunction ·ELEKTA INC.·Product code MUJ·July 28, 2021

3 X 3 SUTURABLE DURAGEN

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES·Product code GXQ·June 5, 2007

ADVANCE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·June 10, 2013

PRIME CARE (R) TRANSCEND MATTRESS

FDA Adverse Event
Malfunction ·PRIMUS MEDICAL LLC·Product code IKY·September 18, 2014

MONACO

FDA Adverse Event
Malfunction ·ELEKTA INC·Product code MUJ·August 25, 2021

EVIS EXERA III VIDEO SYSTEM CENTER

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FET·November 29, 2021

GALAXY G3 MINI 1.5MM X 2CM

FDA Adverse Event
Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·May 20, 2020

OT ULTRA2 METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 26, 2016