18 results · 27ms · Sources: EU EUDAMED, US FDA

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MULTISAFE POWDERED LATEX EXAMINATION GLOVES, NONSTERILE

FDA 510(k)
FDA Class 1 ·General Hospital

Tecomet

FDA UDI
TECOMET INC.·00841435109582·WIRE CUTTER FRONT SIDE, 15° ANGLE TC, WITH SAFE...

Tecomet

FDA UDI
TECOMET INC.·00841435124912·Wire Cutter

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·April 30, 2025

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·April 18, 2025

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·May 21, 2025

ACE CANNULATED CORTICAL BONE SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

SAKURA PREP AI AUTOMATIC LIQUID HANDLING SYSTEM

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

GYNECARE X-TRACT MORCELLATOR

FDA Adverse Event
Injury ·ETHICON, INC.·Product code HET·June 8, 2006

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·September 11, 2024

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·November 19, 2024

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·February 27, 2025

.062 WIRE CUTTER W/ SAFTY INSRT, ANGLED

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code LXH·June 18, 2025

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 19, 2016

UNKNOWN DEPUY ASR CUP

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·March 8, 2013

ENDURANT ABDOMINAL STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 11, 2011

SECURA DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 9, 2015