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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

REPROCESSED TROCARS, MODEL B5LT AND CB5LT

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

Zavation

FDA UDI
Zavation LLC·00842166183865·TRIAL SPACER, 0°, 10x22x60mm

OsteoMed

FDA UDI
OSTEOMED LLC·00845694001465·Extended Y Plate

Orthoblast II Paste

FDA UDI
ISOTIS ORTHOBIOLOGICS, INC.·10889981055615·OrthoBlast II Paste, 8cc - derived from selecte...

Monkey Rings™ External Fixation System

FDA UDI
Paragon 28, Inc.·00889795115881·Threaded Rod, 80

SEALED CALL CORD, 1/4"PLUG, 8FT

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828131292·SEALED CALL CORD, 1/4"PLUG, 8FT

SEALED CALL CORD, 1/4" PLUG, 8FT

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828131285·SEALED CALL CORD, 1/4" PLUG, 8FT

INSTANT-VIEW MORPHINE (2000) URINE CASSETTE TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

ASNIS III CANNULATED SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ONYX AVM

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·April 21, 2011

ONYX

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·January 23, 2013

ONYX, AVM

FDA Adverse Event
Death ·EV3 NEUROVASCULAR·Product code MFE·May 30, 2013

ONYX AVM

FDA Adverse Event
Death ·EV3 NEUROVASCULAR·Product code MFE·March 31, 2011

ONYX

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·December 20, 2012

ONYX AVM

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·May 11, 2011

Widex

FDA UDI
Widex A/S·05706069305067·RC4 version 1 (Fashion grey )

ONYX

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·January 22, 2013

INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022, 130023 AND 130024

FDA 510(k)
FDA Class 2 ·General Hospital

ONYX, AVM

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·December 6, 2011

ONYX

FDA Adverse Event
Injury ·EV3 NEUROVASCULAR·Product code MFE·January 23, 2013