151 results
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30ms
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Sources: EU EUDAMED, US FDA
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·HELIOS II ABLATION CATHETER
MedGyn Pessary Ring w/support #4
FDA UDI
MEDGYN PRODUCTS, INC.·M803050029·Pessary ring is used to treat uterine prolapse.
LATERALIZED AND AUGMENTED BASEPLATE
FDA UDI
FX SOLUTIONS·03701037316801·TA6V CEMENTLESS GLENOID BASEPLATE W/ SCREW Ti/H...
Ni-Ti - Archwire
FDA UDI
ORMCO CORPORATION·00889989025408·PREF.LING.ARCH NI-TI LO16 SZ2 PK/10
CARDIOMPO TEST
FDA 510(k)
FDA Class 2
·Immunology
UNK
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
UNK
FDA Adverse Event
Death
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
UNK
FDA Adverse Event
Malfunction
·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017
BRK¿ XS TRANSSEPTAL NEEDLE, 71 CM LENGTH
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DRC·July 27, 2023
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·EUFLEXXA (1% SODIUM HYALURONATE)
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·DEFLUX INJECTABLE GEL
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·April 10, 2013
CAPSURE SP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·May 8, 2008
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 1, 2011
PRESTIGE(TM) CERVICAL DISC SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MJO·February 25, 2019
PRESTIGE CERVICAL DISC SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MJO·January 28, 2020
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·Euflexxa (1% Sodium Hyaluronate)
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·DEFLUX
Agent, Bulking, Injectable For Gastro-Urology Use
FDA Pre-Market Approval
FDA Class 3
·DEFLUX INJECTABLE GEL
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·EUFLEXXA