30 results
·
28ms
·
Sources: EU EUDAMED, US FDA
AESCULAP NEURO PATTIES
FDA 510(k)
FDA Class 2
·Neurology
OsteoMed
FDA UDI
OSTEOMED LLC·00845694000741·2.4mm x 6mm Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694018678·2.4mm x 6mm Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694029117·2.4mm x 6mm Screw, Sterile
2.0MM X 4MM AUTO-DRIVE SCREW
FDA Adverse Event
Malfunction
·OSTEOMED, LLC·Product code HWC·June 7, 2022
OsteoMed
FDA UDI
OSTEOMED LLC·00845694066761·HPS 2.4 x 6mm Lag Screw Sterile Qty 5
OsteoMed
FDA UDI
OSTEOMED LLC·00845694054652·2.4mm x 6mm Screw Sterile Qty 5
ACCESS SEQUESTRATION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
MITEK 2GII MENISCAL REPAIR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BHR MODULAR HEAD 46MM
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code KWY·January 4, 2018
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
56MM AND R3 ACETABULAR SHELL
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBL·September 14, 2018
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 16, 2013
BENGAY MOIST HEAT THERAPY
FDA Adverse Event
JOHNSON AND JOHNSON GROUP OF CONSUMER COMPANIES·Product code IMD·June 13, 2008
STENOSCOP
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·April 12, 2011
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024
Bentson PTFE Wire Guide, Guidewire, Global Product Number G14589, G14590
FDA Enforcement
Class II
·Terminated·Cook Inc.·February 12, 2020
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025