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

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Needleless Connector

FDA 510(k)
FDA Class 2 ·General Hospital

VERSALOOP™ XL Straight Guide for 1.5mm Anchor XL, Sawtooth

FDA UDI
T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION·10818674025062·

10PW - Penn Power & Light

FDA UDI
Certified Safety Manufacturing, Inc.·00766588012179·10PW - Penn Power & Light

Hayden Medical

FDA UDI
Hayden Medical, Inc.·00840319721872·Cinelli Osteotome 6-1/2" (16.3cm), 14mm cut, do...

neoWave LS

FDA UDI
XENIX MEDICAL LLC·00818345024007·PADDLE SPREADER, 17MM

VIDAS D-DIMER EXCLUSION II 60T

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code DAP·June 19, 2020

4 PORT, 4 WAY STOPCOCK

FDA 510(k)
FDA Class 2 ·General Hospital

SONICSTIMU COMBO THERAPEUTIC DEVICE

FDA 510(k)
FDA Class 2 ·Physical Medicine

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 8, 2023

T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY (WITH T:CONNECT MOBILE APP)

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·January 16, 2025

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

LM

FDA Adverse Event
Malfunction ·YANGZHOU MEDLINE INDUSTRY CO, LTD.·Product code MEG·March 25, 2021

PUMP MMT-712LNAL PRDGM INS CL EN US LN

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code LZG·October 22, 2008

HEARTSTART MRX-EMS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 27, 2013

IN TOUCH ZU

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·July 11, 2011

NV GXL LINER NEUTRAL, 36MM ID, GROUP 2 CUPS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JDI·September 28, 2022

SHOULDER SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 27, 2024

UNK - IMPLANTS

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·October 28, 2019

UNK - IMPLANTS

FDA Adverse Event
Injury ·DEPUY MITEK LLC US·Product code MAI·October 28, 2019

Surpria 64: Software Version V3.11, V3.22

FDA Enforcement
Class II ·Ongoing·FUJIFILM Healthcare Americas Corporation·September 21, 2022