15 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TERUMO IMUGARD
FDA 510(k)
FDA Class 2
·Hematology
VENTURE™ Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902989254·PLATE 9790105 ANT CERV PLATE ASSY 105MM
VENTURE™ Anterior Cervical Plate System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000890308·PLATE 9790105 ANT CERV PLATE ASSY 105MM
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199274·AK3 PS Notch Reamer Guide Size 5/4+
SurgyCut
FDA UDI
U.S. SURGITECH INC.·00810014631134·
SurgyCut
FDA UDI
U.S. SURGITECH INC.·00810014632155·SurgyCut J - Hook Foot Control Electrode, 5mm/45cm
discovery®
FDA UDI
DENTAURUM GmbH & Co.KG·J011790105000·discovery® Bracket with hook, - 2° Torque, + 13...
LUPOTEK KCT
FDA 510(k)
FDA Class 2
·Hematology
ZOOM Aspiration Pump
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 5, 2014
ATTAIN OTW
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·August 5, 2010
BD ALARIS¿ EXTENSION SET
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021
UNSPECIFIED BD INFUSION SET
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022
PROPONENT DR SL (Model L201)
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025