1,141 results · 22ms · Sources: EU EUDAMED, 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