38 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROXENON 350, MODEL 902XX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sklar®
FDA UDI
SKLAR CORPORATION·10649111091322·MACINTOSH END STD LG ADLT SZ 5
ACUMATCH L-SERIES CEMENTED FEMORAL STEM, MODEL SIZE 1
FDA 510(k)
FDA Class 2
·Orthopedic
CORRECT PLUS
FDA 510(k)
FDA Class 2
·Dental
KeyLift™
FDA UDI
FLOSPINE LLC·B1830712181120·KeyLift XS 18mm Lg x 12mm H
KeyLift™
FDA UDI
FLOSPINE LLC·B1830712181160·KeyLift XS 18mm Lg x 16mm H
KeyLift™
FDA UDI
FLOSPINE LLC·B1830712181140·KeyLift XS 18mm Lg x 14mm H
KeyLift™
FDA UDI
FLOSPINE LLC·B1830712181100·KeyLift XS 18mm Lg x 10mm H
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
VERCISE CARTESIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·May 23, 2023
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
COCR FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·February 23, 2018
S5 SENSOR MODULE FOR BUBBLE DETECTOR
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016