33 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ATHENA PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Corin BiPolar-i
FDA UDI
CORIN LTD·05056139233920·Acetabular Trial Ø46
OsteoMed
FDA UDI
OSTEOMED LLC·00845694040129·PrimaLIF 6mm Kerrison Rongeur, Up
Integrity-SI Fusion System
FDA UDI
Lincotek Medical LLC·B57112521110046D0·10 x 45 mm SI Implant Fully Threaded with HA Co...
M SEIRES PATIENT MONITOR MODEL M66, M69, M8000, M9000, M7000
FDA 510(k)
FDA Class 2
·Cardiovascular
NUVOLASE 532 MEDICAL LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RD SET YI
FDA Adverse Event
Malfunction
·MASIMO - 52 DISCOVERY·Product code DQA·March 29, 2021
RD SET DCI
FDA Adverse Event
Malfunction
·MASIMO - 15750 ALTON PKWY·Product code DQA·February 10, 2023
Trilogy®
FDA UDI
Zimmer, Inc.·00889024636897·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024636903·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360358·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024636880·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360372·
Trilogy®
FDA UDI
Zimmer, Inc.·00889024360365·
ELECTRONIC GAS BLENDER
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025
STOCKERT S3 GAS BLENDER
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·May 13, 2013
SYBRONPRO XRT
FDA Adverse Event
Injury
·EBI INC.·Product code DZE·June 1, 2011
CLEARGLIDE PRECISION BIPOLAR DEVICE
FDA Adverse Event
DATASCOPE CORP.·Product code GEI·August 7, 2008
S3 GAS BLENDER SYSTEM
FDA Adverse Event
Malfunction
·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017