1,141 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PERIFIX CATHETER CONNECTOR
FDA 510(k)
FDA Class 2
·Anesthesiology
Safco T&F Bur - 12 Bladed
FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310220193·Safco T&F bur - 12 bladed, carbide, #7902 needl...
infinity OCTAGON BL NC Healing abutment, conical Ø3.6 mm GH 5.0 mm
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50220191·BL NC Healing abutment, conical Ø3.6 mm GH 5.0 ...
36M - Class B 21 - Metal
FDA UDI
Certified Safety Manufacturing, Inc.·00766588620190·36M - Class B 21 - Metal
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710310220190·Talar Osteotmy Guide, 22mm x 19mm
COLOR BUFFED (CB) DDH FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET
FDA 510(k)
FDA Class 2
·Cardiovascular
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS LLC·Product code OYC·January 4, 2019
NUCLEUS HYBRID L24
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code PGQ·July 1, 2019
ASSURITY PLUS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWP·July 2, 2019
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·March 26, 2013
ADVANTAGE SERIES 29 OBS 10/04
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·March 10, 2011
IVS TUNNELLER
FDA Adverse Event
Injury
·BALLYMONEY - USS·Product code FTL·March 31, 2008
ROUND BLAKE HUBLESS SILICON DRAINS - 3/4 FLUTED
FDA Adverse Event
Injury
·ETHICON INC.·Product code KOG·October 23, 2014
ROUND BLAKE HUBLESS SILICON DRAINS - 3/4 FLUTED
FDA Adverse Event
Injury
·ETHICON INC.·Product code KOG·October 23, 2014
ROUND BLAKE HUBLESS SILICON DRAINS - 3/4 FLUTED
FDA Adverse Event
Injury
·ETHICON INC.·Product code KOG·October 23, 2014
AMS INFLATABLE PENILE PROSTHESIS WITH INHIBIZONE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FHW·January 14, 2020
Smiths Medical CADD" Yellow Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included 100mL, Product Code 21-7300-24
FDA Enforcement
Class II
·Ongoing·ICU Medical Inc.·September 10, 2025
NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM STRAIGHT ELECTRODE
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·April 1, 2019
BIA400 IMPLANT 4MM W ABUTMENT 8MM
FDA Adverse Event
Injury
·Product code MAH·May 1, 2019