33 results
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34ms
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Sources: EU EUDAMED, US FDA
EVRON GEL
FDA 510(k)
FDA Class 1
·General Hospital
VERTE-STACK® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074018676·SPACER 2961222 CAPS VS PK VBS END 22X12
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295235972·P.F.C. SIGMA POSTERIOR-LIPPED TIBIAL INSERT TRI...
Sklar Instruments
FDA UDI
SKLAR CORPORATION·10649111246289·ECONO STERILE UTILITY SCISS PRPL ST CS25 7"
Empower Tube
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746197611·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-10 R...
Empower Tube
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746201608·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-14 R...
Empower Tube
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746201592·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-10 R...
Empower SL Molar
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746030635·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-10 R...
Empower SL Molar
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746030642·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-14 R...
Empower Tube
FDA UDI
AMERICAN ORTHODONTICS CORPORATION·00190746198144·DB TUBE SL EMPOWER UR 1ST MOL 022/018AUX T-14 R...
SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code MQP·October 30, 2017
INJECTRA INJECTION NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PENTAX MEDICAL ED-3490TK, Video Duodenoscope
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 29, 2016
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·August 24, 2016
NI
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FPA·October 3, 2016
CLEARLINK DUO-VENT CONTINU-FLO SOLUTION SET
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FPA·October 1, 2020
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·May 28, 2014
THERAKOS CELLEX PHOTOPHERESIS SYSTEM
FDA Adverse Event
Malfunction
·THERAKOS·Product code LNR·February 8, 2013
UNIVERSAL DRIVER SHAFT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·December 21, 2010