8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BTL-785S
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DELTA CER HEAD 12/14 32MM +5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LZO·October 11, 2024
ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS
FDA 510(k)
FDA Class 2
·Neurology
TRINGA ULTRASOUND IMAGING SYSTEM, MODEL 50L
FDA 510(k)
FDA Class 2
·Radiology
PFC SIGMA DIS AUG8MM, S2.5, RGHT
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC·Product code JWH·November 14, 2008
STARCLOSE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·September 2, 2011
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MRU·July 18, 2013
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·December 13, 2020