39 results · 27ms · 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.

XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020

FDA 510(k)
FDA Class 2 ·Microbiology

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017

IMAGER II UROLOGY TORQUE CATHETER, MODEL 40030X1, 40040X1, AND 40050X1

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

SAFE-POINT VAC, SAFE-POINT M-D BLOOD COLLECTION SYSTEMS

FDA 510(k)
FDA Class 2 ·General Hospital

PROCEED MULTI-LAYER LAMINATE MESH

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 16, 2006

PROCEED MULTI-LAYER LAMINATE MESH

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 26, 2006

PROCEED MULTI-LAYER LAMINATE MESH

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 26, 2006

PROCEED MULTI-LAYER LAMINATE MESH

FDA Adverse Event
Injury ·ETHICON, INC.·Product code FTL·June 27, 2006

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·August 3, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 11, 2020

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NKB·February 3, 2010

TSRH SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code NKB·February 3, 2010

ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·December 22, 2017

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 26, 2019

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2018

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 2, 2019

NEXGEN STEMMED TIBIAL COMPNENT

FDA Adverse Event
Injury ·ZIMMER·Product code JWH·March 28, 2013

CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·March 28, 2011

J-VAC RESERVOIR

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code GCY·April 17, 2008

TSRH SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·May 12, 2017