8 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LAPAROTOMY PADS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
OPUS 10 (WITH TOOTH WHITENING APPLICATION), MODEL 2ND
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Arthrex FiberTak Suture Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
COBAS C 503 ANALYTICAL UNIT
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·November 18, 2025
M2A-MAGNUM MOD HEAD SZ 42MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 15, 2014
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code NBW·August 23, 2010
RESTORE SENSOR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 30, 2014