22 results · 23ms · Sources: EU EUDAMED, US FDA

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DIXI Medical Microdeep Micro-Macro Depth Electrodes

FDA 510(k)
FDA Class 2 ·Neurology

SprintRay Ceramic Crown - A3

FDA UDI
Sprintray, Inc.·00850039704444·Intended for the fabrication of individual and ...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112502·BARRON VACUUM TREPHINE 7.75MM

E-A-RLINK™

FDA UDI
3M COMPANY·10080529191288·3M(TM) E-A-RLINK(TM) 3B Foam Eartip small size,...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112625·BARRON CORNEAL PUNCH 7.75MM

BESTEX POWDER-FREE LATEX EXAM GLOVES WITH LABELING CLAIM. (50 MICROGRAMS OR LESS)

FDA 510(k)
FDA Class 1 ·General Hospital

DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAM GLOVES WITH ALOE VERA, GREEN COLOR

FDA 510(k)
FDA Class 1 ·General Hospital

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 13, 2024

XEN 45 GTS

FDA Adverse Event
Injury ·Product code KYF·October 7, 2021

BD INTIMA-II¿ Y 18GAX1.16IN PRN EC SLM NPVC

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·May 2, 2019

ARTHREX PUSHLOCK 4.5 MM X 1 8.5MM

FDA Adverse Event
Injury ·ARTHREX, INC·Product code MBI·October 10, 2008

SECURA DR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

PLUM A+ 3 MEDNET SW

FDA Adverse Event
Death ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 26, 2013

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2023

BD PLASTIPAK ¿ 3-PIECE SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 6, 2022

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·March 1, 2023

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·March 1, 2023

CHECK-IT

FDA Adverse Event
Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·February 4, 2023

STEALTHSTATION S7

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·May 27, 2021