65 results
·
45ms
·
Sources: EU EUDAMED, US FDA
Arch Therapeutics Inc.
Manufacturer
🇺🇸 United States
ARCH THERAPEUTICS
FDA registration
ARCH THERAPEUTICS·2 products·🇺🇸 United States
RESTORE ADVANCED RECHARGEABLE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·May 28, 2010
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·March 26, 2015
THERAPEUTIC BOOT
FDA Adverse Event
Injury
·BREG, INC.·Product code ITW·January 12, 2026
VALIANT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·March 5, 2015
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 23, 2008
IMPLANT, FIXATION DEVICE, SPINAL
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code JDN·June 18, 2015
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 15, 2011
DR SCHOLL'S PAIN RELIEF ORTHOTICS (PRO) FOR ARCH
FDA Adverse Event
Other
·Product code KNP·October 15, 2014
NONTEMPLATE ALIGNER ARCH
FDA Adverse Event
Injury
·DENTSPLY SIRONA ORTHODONTICS INC.·Product code NXC·August 23, 2022
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 21, 2010
DEEP BRAIN STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 3, 2008
PRECISE PRO RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIM·December 6, 2011
STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·February 6, 2017
RUNWAY 6 FRENCH FR-4 GUIDE CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code DYB·August 19, 2004
ITREL 3
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·December 19, 2012
OLYMPUS
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code KNS·December 5, 2007
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·April 11, 2014
TALENT TAA
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·June 3, 2014