27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DANIELS SHARPSMART REUSABLE SHARPS CONTAINER
FDA 510(k)
FDA Class 2
·General Hospital
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040072561·Steel Bur RA 36
Straumann
FDA UDI
Preat Corporation·00842092122419·Straumann® TL WN-compatible Non-Engaging Verifi...
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00143371·
Fitbone Trochanteric
FDA UDI
ORTHOFIX SRL·18059015376425·FITBONE TROCHANTERIC TRIAL NAIL L337MM D11MM
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001337·artVeneer life upper anteriors, BOL, C2
OptiMesh Multiplanar Expandable Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7401001337·TLIF Portal Anchor, Angled 2mm
MAMMARY PROSTHESIS, 240 CC
FDA Adverse Event
MCGHAN MEDICAL CORP.·Product code FTR·February 17, 1994
MODIFICATION TO EBI SPINELINK SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MTP DISPOSABLE TROCAR VALVES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AVEIR¿ DELIVERY CATHETER
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code PNJ·September 25, 2025
BIPOLAR MACRO FORCEPS D:5/ 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·April 6, 2015
BIPOLAR MARYLAND DISS.FCPS 5MM 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·March 9, 2015
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014
JAW INS. BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015
MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015
APTIMA SARS COV-2
FDA Adverse Event
Malfunction
·HOLOGIC, INC.·Product code QJR·September 23, 2022
CORTSCR Ø1.5 SELF-TAP L10 TAN
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code MQN·March 13, 2013
COULTER® PREPPLUS 2 CYTOMERTY
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LOQ·February 25, 2011