7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
ASPIRATING ENDO OCULAR PROBE
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
PLIF Allograft
FDA UDI
Seaspine Orthopedics Corporation·10889981087579·11mm Box Cutter
BASIC AND DOMINANT FLEX SUCTION PUMPS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BIOARC SP SLING KIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BREEZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·January 25, 2013
EON IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL -NEUROMODULATION·Product code LGW·November 18, 2010
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEATHCARE CORPORATION·Product code FKX·July 11, 2014