22 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MULTIFIX S KNOTLESS FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LOCATOR R-Tx
FDA UDI
Zest Anchors, LLC·00840481120947·LOCATOR R-Tx Abutment For UF(II) Regular/Wide I...
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319704929·Foerster Sponge (Ring) Forceps 7" (17.5cm), ser...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197056151·Herrick Pedicle Clamp
angled...
INNERVUE DIAGNOSTIC SCOPE SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
OTIS -C PLUS
FDA 510(k)
FDA Class 2
·Orthopedic
UniTip Catheter
FDA UDI
Unisensor AG·07640172971345·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973639·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971338·
UniTip Catheter
FDA UDI
Unisensor AG·07640172973219·
THE X-STOP® INTERSPINOUS SPACER
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 11, 2014
THE X-STOP® INTERSPINOUS SPACER
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 10, 2014
THE X-STOP® INTERSPINOUS SPACER
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NQO·July 10, 2014
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 31, 2013
LIGASURE IMPACT
FDA Adverse Event
Malfunction
·COVIDIEN LP (VALLEYLAB)·Product code GEI·June 16, 2011
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS CORP.·Product code LFR·August 28, 2008
BD POSIFLUSH¿ SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·November 22, 2022
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 27, 2015
NEOPUFF INFANT RESUSCITATOR
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTL·January 6, 2015
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·April 8, 2016