151 results · 30ms · Sources: EU EUDAMED, US FDA

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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