30 results · 25ms · Sources: EU EUDAMED, US FDA

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CONQUEST 40 PTA DILATATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

M-Flex®

FDA UDI
DIVERSATEK HEALTHCARE, INC.·00816734020203·Blue Silicone Tungsten Maloney Esophageal Dilat...

Logical Cup Liner

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215054199·

Logical 20° Hooded Liner

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215009458·

OrthoMedFlex

FDA UDI
ORTHOMEDFLEX LLC·M7161111206600·Liner, 36-60/68mm (20° Hood)

INFRARED EAR THERMOMETER MODEL DR. SCHVEN ICT-1000

FDA 510(k)
FDA Class 2 ·General Hospital

HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO

FDA 510(k)
FDA Class 2 ·General Hospital

VENTO XLPE Liner

FDA UDI
AMPLITUDE SAS·03701089514620·

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·March 25, 2022

BIOLOX DELTA CER LNR 36MM E

FDA Adverse Event
Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

RINGLOC-X E1 H/W 56/36MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·April 27, 2026

BIOLOX DELTA CER LNR 40MM G

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·April 27, 2026

20G X 1.16IN (1.1 X 30 MM) INSYTE AUTOGUARD BC

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 11, 2019

BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CATHETER

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 5, 2019

TRIATHLON PS X3 TIBIAL INSERT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·May 20, 2013

TEGO CONNECTOR

FDA Adverse Event
Malfunction ·ICU MEDICAL, INC.·Product code FPA·July 28, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 10, 2011

AVAN E1 INSERT 28 S 52

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LZO·March 6, 2025

BIOLOX DELTA CER LNR 32MM E

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·September 8, 2025

RINGLOC BIPOLAR VIVACIT-E

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·September 10, 2025