39 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AUTOBAHN Nailing System
FDA 510(k)
FDA Class 2
·Orthopedic
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292558·
NA
FDA UDI
KEY SURGICAL, INC.·10849771048913·K-Wires, Double trocar, .054-inch (1.4mm) diame...
Cranial Fusion
FDA UDI
Life Spine, Inc.·00190837085261·
K-Wire w. double end trocarpoint 1.40mm/127mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM711080·K-Wire w. double end trocarpoint
1.40mm...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484092·K-Wire w. double end trocarpoint _x000D_...
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009703·
BD MICROLANCE¿ 3 NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·June 7, 2019
TEXIUM SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
ERBE ESU MODEL VIO 100 C WITH ACCESSORIES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD MICROLANCE¿ 3 NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·July 1, 2019
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009758·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009734·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009727·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009710·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072009741·
BD NEEDLE 30GA 1/2IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·July 23, 2019
BD MICROLANCE¿ NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·July 31, 2019
ellex I.Science iTRACK 250A, Canaloplasty Microcatheter Kit, for single use, REF iT-250A, Rx. The firm name on the label is Ellex iScience, Inc., Fremont, CA. Used in ophthalmic surgery.
FDA Enforcement
Class II
·Terminated·Ellex iScience, Inc.·October 10, 2018
INSERT-HANDLE F/UFN/CFN
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code LXH·June 14, 2013