38 results · 25ms · Sources: EU EUDAMED, 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