26 results
·
27ms
·
Sources: EU EUDAMED, US FDA
RT-PLUS KNEE ADDITIONAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
AOS MODULAR NAIL 13.0mm x 34cm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665003314·
COMBINATION GEL-INFLATABLE MAMMARY PROSTHESES
FDA Adverse Event
Injury
·AMERICAN HEYER-SCHULTE·Product code FTR·April 17, 1998
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475652·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475843·
PedFuse®
FDA UDI
SPINEFRONTIER, INC.·00190361012412·PedFuse Remind LES, Quad, 6.0mm x 40mm
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475638·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475683·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475669·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475645·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033475676·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130400·ROD REDUCER, AXIAL
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 15, 2025
NA
FDA UDI
STERILMED, INC.·10888551026642·BUR TAPERED DIAMOND COARSE
MODULITH LITHOTRIPSY, MODEL SLK FOR THE FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULI
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OBC-149 BREAST ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
ILET BIONIC PANCREAS
FDA Adverse Event
Malfunction
·BETA BIONICS, INC.·Product code QFG·May 11, 2026
ACCU-CHEK ® INFORM METER
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·March 20, 2013
LEGEND FOOTED ATTACHMENT
FDA Adverse Event
Malfunction
·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·March 10, 2011
AA
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWB·March 13, 2008