19 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AlloX2 Pro Tissue Expanders
FDA 510(k)
FDA Unclassified
·Unknown
NA
FDA UDI
Richard Wolf GmbH·04055207014455·TRACHEAL SCOPE-TUBE ID 12MM model Hemer, OD 13...
EXPRESSEW
FDA UDI
Medos International Sàrl·10886705003655·EXPRESSEW III w/ Hook Flexible Suture Passer Re...
ALEUTIAN® Interbody Systems
FDA UDI
VB Spine LLC·10888857522480·Trial Size 13x16x12 mm, 20°
RATCHET SCREWDRIVER HANDLE
FDA UDI
Biomet Orthopedics, LLC·00887868447341·
Tandry Locking Plate System
FDA UDI
MICROWARE PRECISION CO., LTD.·04719873097203·Cortex Screw 1.5mm, 24mm, Hexalobular
RATCHET SCREWDRIVER HANDLE
FDA UDI
Biomet Orthopedics, LLC·00887868024399·
VENFLON PRO 1.8MM X 45MM
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·April 15, 2021
NUMED COEFFICIENT PTV CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
Synergy Gold (SG) Portable (Models MM011450 and MM011460)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CELL-DYN WBC REAGENT A
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·October 30, 2008
GENESIS 8-CHANNEL RECHARGEABLE IPG
FDA Adverse Event
Other
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2011
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 9, 2013
MITEK EXPRESSEW III NEEDLE
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code LXH·August 17, 2015
EXPRESSEW III W/O HOOK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code LXH·November 12, 2018
AVIATOR PLUS PTA DILATATION CATHETER
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code LIT·August 9, 2012
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIM·August 9, 2012
ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NTE·August 9, 2012
EXPRESSEW III W/HOOK
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code LXH·January 30, 2019