91 results
·
18ms
·
Sources: EU EUDAMED, US FDA
INFUSION ADAPTER C100
FDA 510(k)
FDA Class 2
·General Hospital
OsteoMed
FDA UDI
OSTEOMED LLC·00845694039956·PrimaLIF 3mm Pituitary Rongeur, Up
MIRABAY
FDA UDI
Mirabay Orthodontics Corp.·05061075023030·KLEOS 2 PSL METAL MBT 022 UL45 HK PK5 UNI
Avalign
FDA UDI
Avalign Technologies, Inc.·00190776020927·Keyhole Bracket
Powered Loading System (PLS) (Component)
FDA UDI
LIFEPORT, LLC·00810050862004·INSTALL RAIL ASSY NO MOD * (PLS)
MTF NEW BONE VOID FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
PROFILE-V MEDTOXSCAN DRUGS OF ABUSE TEST SYSTEM AND 12 DRUGS TEST SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
RESPIRONICS
FDA Adverse Event
Malfunction
·Product code MNT·April 8, 2021
RADICAL 7
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·December 18, 2014
RADICAL 7
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·December 18, 2014
MG II®
FDA UDI
Zimmer, Inc.·00889024435834·
MG II®
FDA UDI
Zimmer, Inc.·00889024435797·
MG II®
FDA UDI
Zimmer, Inc.·00889024435803·
MG II®
FDA UDI
Zimmer, Inc.·00889024435841·
MG II®
FDA UDI
Zimmer, Inc.·00889024435810·
MG II®
FDA UDI
Zimmer, Inc.·00889024435827·
RADICAL-7 COLOR SCREEN HANDHELD
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·May 29, 2015
RDS3 DOCKING STATION
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·September 17, 2014
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·EVERFLEX SELF-EXPANDING PERIPHERAL STENT SYSTEM (EVERFLEX)
VANGUARD SSK PS TIBIA BEARING 24X71/75
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·May 13, 2013