6,550 results · 34ms · Sources: EU EUDAMED, US FDA

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Epsilon USA

FDA UDI
EPSILON EYE CARE PRIVATE LIMITED·G346EMF14P0·Micro Handle Colibri 0.12mm 1x2 Teeth Forceps W...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613082871·Micro Handle Colibri Forceps, Titanium, 0.12mm,...

Epsilon USA

FDA UDI
EPSILON EYE CARE PRIVATE LIMITED·G346EMF140·Micro Handle Colibri 0.12mm 1x2 Teeth Forceps (...

ORTHO DEVELOPMENT ORION-I EMF SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ENDOSCOPIC MONOPOLAR FORCEPS-SCISSORS, EMF-2000 TO 2999,ENDOSCOPICS MONOPOLARFOEPS-GRASPERS, EMF-3000 TO 3999, ENDOSCOPO

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

NEUROSTIMULATOR IMPLANT

FDA Adverse Event
Malfunction ·UNK·Product code LGW·February 9, 2022

SPINE STIMULATIOR

FDA Adverse Event
Injury ·UNK·Product code LGW·April 9, 2026

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code MRU·December 28, 2017

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·May 29, 2018

EMF PAL II MAIN GENERATOR AND IRRIGATION UNITS AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

MRI

FDA Adverse Event
Injury ·PICKER INTL·Product code LNH·April 12, 1994

MEDTRONIC

FDA Adverse Event
Malfunction ·Product code LGW·July 18, 2011

MRI

FDA Adverse Event
Injury ·GE HEALTHCARE MANUFACTURING LLC·Product code LNH·March 23, 2026

STRYKER TRIDENT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS/HOWMEDICA OSTEONICS CORP·Product code LPH·September 8, 2025

PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

FDA Adverse Event
Injury ·STRYKER ORTHOPEDICS/HOWMEDICA OSTEONICS CORP·Product code LPH·September 8, 2025

PUMP MMT-1780KPK 670G PATHWAY BLACK MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 14, 2022

PACEMAKER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWP·July 29, 2021

STRYKER SPINE XIA 4.5 TITANIUM ROD

FDA Adverse Event
Injury ·STRYKER SPINE·Product code JDN·May 28, 2008

QUANTUM

FDA Adverse Event
Malfunction ·INTERMEDICS, INC.·Product code DXY·September 15, 1994

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 21, 2008