15 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Vsmilehappyzir Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank
FDA 510(k)
FDA Class 2
·Dental
Sklar®
FDA UDI
SKLAR CORPORATION·10649111348006·STEVENS TENOT DEL STR BB 4 1/2
CAPTURE-R READY INDICATOR RED CELLS
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·November 18, 2014
TM "Soloventex" 221-242 XL
FDA UDI
REABILITIMED TOV·04823097718551·Men's closed-toe socks, 2nd compression class 2...
TM "Soloventex" 221-242 M
FDA UDI
REABILITIMED TOV·04823097718537·Men's closed-toe socks, 2nd compression class 2...
TM "Soloventex" 221-242 XXL
FDA UDI
REABILITIMED TOV·04823097718568·Men's closed-toe socks, 2nd compression class 2...
TM "Soloventex" 221-242 S
FDA UDI
REABILITIMED TOV·04823097718520·Men's closed-toe socks, 2nd compression class 2...
TM "Soloventex" 221-242 L
FDA UDI
REABILITIMED TOV·04823097718544·Men's closed-toe socks, 2nd compression class 2...
PORTALLOY 54
FDA 510(k)
FDA Class 2
·Dental
Promisemed Sterile Hypodermic Syringes, Verifine Sterile Hypodermic Syringes
FDA 510(k)
FDA Class 2
·General Hospital
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 5, 2008
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·August 16, 2011
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·July 11, 2013
OT VERIO IQ METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013
cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V
FDA Enforcement
Class II
·Terminated·Roche Diagnostics Corporation·March 14, 2018