22 results
·
22ms
·
Sources: EU EUDAMED, US FDA
PSYCHEMEDICS PHENCYCLIDINE EIA
FDA 510(k)
FDA Unclassified
·Unknown
SureFISH IGH BA P200
FDA UDI
AGILENT TECHNOLOGIES, INC.·05700574008949·SureFISH IGH BA P200
MAXCUT CARBIDE BUR (100/pk) FG 245
FDA UDI
SCOTT'S DENTAL SUPPLY L.L.C.·D77811119281·MAXCUT CARBIDE BUR (100/pk) Shape: Amalgam Prep...
VENTRALEX ST HERNIA PATCH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HYDROTOWER ARTHROSCOPIC ADMINISTRATION TUBING SET, MODEL 7-460-05
FDA 510(k)
FDA Class 2
·General Hospital
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019
GELB MOUTHGUARD
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·April 10, 2019
ASTRON CLEAR SPRINT
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 14, 2020
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 17, 2019
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 16, 2019
ASTRON CLEAR SPLINT
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 22, 2020
ASTRON CLEAR SPLINT LOWER
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 30, 2020
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·May 4, 2020
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·May 14, 2013
ACCU-CHEK ® MULTICLIX
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·June 2, 2011
SMART CONTROL NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code FGE·August 11, 2008
ASTRON CLEAR SPLINTS
FDA Adverse Event
Injury
·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 2, 2020
HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP
FDA Adverse Event
Death
·HEARTWARE, INC.·Product code DSQ·April 21, 2025