11 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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WET-PREP
FDA 510(k)
FDA Class 2
·Dental
SURGISTAR
FDA UDI
SURGISTAR, INC.·00878799004031·
SURGISTAR, INC.
FDA UDI
SURGISTAR, INC.·00878799002532·
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295240204·P.F.C. SIGMA DISTAL AUGMENTATION TRIAL SZ 2 8mm
CAPD DISP DISCONNECT, UV FLASH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code KDJ·May 23, 2008
OMRON AUTOMATIC BLOOD PRESSURE MONITOR WITH COMFIT CUFF, MODEL HEM 780 N3
FDA 510(k)
FDA Class 2
·Cardiovascular
Torcon NB Advantage Catheters
FDA 510(k)
FDA Class 2
·Cardiovascular
XIA 3 TITANIUM POLYAXIAL SCREW DIA 7.5 X 70 MM
FDA Adverse Event
Malfunction
·STRYKER SPINE-SWITZERLAND·Product code MNH·February 14, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 28, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·January 14, 2011
BEACON TIP TORCON NB ADVANTAGE ANGIOGRAPHIC CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code DQO·November 26, 2025