38 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CarboClear® Pedicle Screw System, CarboClear® II Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
DJO SURGICAL
FDA UDI
Encore Medical, L.P.·00190446923091·SPECIAL EMPOWR KNEE 2 DEG VARUS, TIBIAL RECUT G...
Blade Handle
FDA UDI
KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG
AUROPAL 60
FDA 510(k)
FDA Class 2
·Dental
VASCULAR GRAFT TUNNELER-STANDARD CURVE, MID CURVE, FULL CURVE, SHORT STANDARD CURVE, VASCULAR GRAFT TUNNELER ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
ELLUME COVID-19 HOME TEST
FDA Adverse Event
Malfunction
·ELLUME LIMITED·Product code QKP·December 16, 2021
ENDOTAK DSP
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·August 8, 2000
VALIANT CAPTIVIA UNK
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·December 18, 2019
VALIANT CAPTIVIA UNK
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·December 18, 2019
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·October 30, 2020
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 17, 2020
INSPIRE OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·March 4, 2026
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·September 13, 2019
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·September 10, 2019
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·July 10, 2019
UNKNOWN ENDO GIA INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·July 10, 2019
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·July 31, 2019
AXIOM REG IMPLANT
FDA Adverse Event
Injury
·ANTHOGYR·Product code DZE·September 11, 2019
MINICAP PD TRANSFER SET (EASY-LOCK) WITH TWIST CLAMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·October 21, 2008
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011