17 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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W-55 (METHAFILCON A) CLEAR AND VISIBILITY TINTED LENS BLANK AND HORIZON 55 SOFT (CLEAR) AND HORIZON 55 WESTINT (TINTED)
FDA 510(k)
FDA Class 2
·Ophthalmic
Tubifast®
FDA UDI
Mölnlycke Health Care AB·05055158000780·Tubifast Vest 8 - 11 yrs x 6
SPECIALIST
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295253761·SPECIALIST REVISION SLEEVE 24mm
SCOTT'S SELECT MICROHYBRID SYRINGE 4.5 Gm (OPAQUE)
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77819920100·Scott’s Select Microhybrid Composite is indicat...
IMA Cross Bar
FDA UDI
KOROS U.S.A., INC.·10840199542755·IMA Cross Bar
PC ECG, MODEL SE-1010
FDA 510(k)
FDA Class 2
·Cardiovascular
SmoothSkin BARE+
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
WALLSTENT RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code JCT·March 21, 2025
PREMIER ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWQ·August 12, 2011
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·March 3, 2017
PREMIER® ANTERIOR CERVICAL PLATE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 7, 2015
DLT TS CER HD 12/14 36MM +8.5
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JDI·March 7, 2013
MARQUIS DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code LWS·February 15, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 8, 2014
WALLSTENT? RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025
GALAXY G3 XSFT 2MM X 2CM
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code KRD·August 13, 2019