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

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OVision Imaging System

FDA 510(k)
FDA Class 2 ·Radiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777679·LUMBAMED BASIC DORSAL STAYS M SILVER V

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772777624·LUMBAMED BASIC DORSAL STAYS WM SILVER V

7020 CONNECTORS

FDA UDI
HANS RUDOLPH, INC.·00817136022284·CONN 22ID X 22ID 7020 SERIES

Sportex

FDA UDI
Diversified Products, Inc.·00842894170496·

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112601·BARRON CORNEAL PUNCH 7.25MM

BALANCE MICROPLASTY BROACH

FDA UDI
Biomet Orthopedics, LLC·00880304459229·

ACRA-CUT

FDA UDI
ACRA-CUT INC·00810607002754·Disposable Cranial Perforator

Autolith Touch

FDA UDI
NORTHGATE TECHNOLOGIES INC.·00817183020493·Lithotripter, Biliary, BSC

DATEX-OHMEDA TEC 6 PLUS ANESTHESIA VAPORIZER, DATEX-OHMEDA TEC 6 PLUS NAD VARIANT ANESTHESIA

FDA 510(k)
FDA Class 2 ·Anesthesiology

WORKING ELEMENT, RESECTION BUTTON ELECTRODE FOR PLASMA VAPORIZATON, HF-RESECTION ELECTRODE LOOPS AND BANDS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

AUTOLITH TOUCH

FDA Adverse Event
Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·September 25, 2021

PHYSICA TT

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code MBH·December 21, 2023

Disposable Cranial Perforator

FDA UDI
ACRA-CUT INC·00810607000088·Cranial Perforator

PLATE MUELLER HINTON II AGAR

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 26, 2022

ANIMAS INSULIN CARTRIDGE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·April 29, 2016

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 24, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·July 1, 2013

i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300

FDA Recall
Open, Classified ·Abbott Point Of Care Inc.·Product code CHL·August 21, 2025