34 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Neocis Guidance System (NGS) with Yomi Plan v2.0
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113226·VITRECTOMY KNIFE 20GA (BX/5)
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668113264·SIDEPORT KNIFE 1MM ANGLED (BX/5)
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112984·CORNEAL TREPHINE BLADE9.5MM
BRANAN MEDICAL CORPORATION MONITECT COCAINE DRUG SCREEN TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CLEAN 'N' OIL
FDA 510(k)
FDA Class 1
·Dental
FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT
FDA Adverse Event
Injury
·FUJIFILM CORPORATION·Product code FDA·July 25, 2022
UNKN JOURNEY BCS / JOURNEY II BCS KNEE
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·April 30, 2024
KIT IMPLANTABLE SLIM TIP LEAD, 50CM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code PMP·March 8, 2026
TENDRILL STS
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NVN·January 13, 2014
CAPSUREFIX
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 28, 2013
KIT IMPLANTABLE SLIM TIP LEAD, 50CM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code PMP·December 22, 2023
COOL PATH¿ IRRIGATED ABLATION CATHETER
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code OAD·October 25, 2022
STRATA®
FDA Adverse Event
Malfunction
·COVIDIEN LLC·Product code JXG·April 22, 2022
STRATA®
FDA Adverse Event
Injury
·COVIDIEN LLC·Product code JXG·April 22, 2022
EVOLUT PRO PLUS VALVE
FDA Adverse Event
Death
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 12, 2022
FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT
FDA Adverse Event
Injury
·FUJIFILM CORPORATION·Product code FDA·July 21, 2022
MICRA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DYB·February 1, 2023
MICRA AV
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code PNJ·February 16, 2023