31 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set
FDA 510(k)
FDA Class 2
·Cardiovascular
Conventional Lead Apron .5mm Xtra Xtra Large 26 X 42
FDA UDI
Flow X Ray Corporation·00843696123949·Conventional Lead Apron .5mm XXL 26 X 42, Shimm...
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112830·BARRON VACUUM PUNCH 9.5MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112809·BARRON VACUUM PUNCH 8.75MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112960·CORNEAL TREPHINE BLADE8.75MM
ACUMATCH P-SERIES PRESS-FIT PLASMA, ACUMATCH P-SERIES PRESS-FIT, ACUMATCH L-SERIES PRESS-FIT
FDA 510(k)
FDA Class 2
·Orthopedic
VERDICT-II
FDA 510(k)
FDA Class 2
·Clinical Toxicology
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 29, 2025
APTIMA
FDA Adverse Event
Malfunction
·Product code JJC·October 16, 2008
LIBERTY CYCLER SET, SINGEL CONN./EXT.DL
FDA Adverse Event
Malfunction
·REYNOSA MANUFACTURING·Product code FKX·June 28, 2013
SPRINT
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011
ATTUNE PS FEM LT SZ 7 CEM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code OIY·May 25, 2021
ATTUNE PS RP INSRT SZ7 6MM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code NJL·May 25, 2021
ATTUNE RP TIB BASE SZ 8 CEM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code NJL·May 25, 2021
ATTUNE MEDIAL DOME PAT 41MM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code OIY·May 25, 2021
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·June 30, 2021
MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAN·August 25, 2021
VCL+ VIO 36IN 2-0 S/A CT-1
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·September 23, 2021
GYNECARE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTO·August 25, 2021
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Injury
·HEARTWARE, INC.·Product code DSQ·January 28, 2022