27 results · 22ms · Sources: EU EUDAMED, 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