9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TORQUE DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
LP Low Profile
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746090950·DB BKT LP V-SLOT UL CEN 022 T+18 A+5 R=0
OMNI Knee
FDA UDI
Omni Life Science, Inc.·00841690101611·Ultra Tibial Insert CS, Size 3 x 12mm
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515245075·Weil Blakelsey Fcp ang 30 deg left, 3.5mm, sz 0
CHEMOSITE IMPLANTABLE DRUG DELIVERY
FDA 510(k)
FDA Class 1
·General Hospital
RETRACTOR RODS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·January 30, 2013
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 13, 2010
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 15, 2014