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

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SIDEKICK AND USHER SUPPORT CATHETERS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Spherodon +

FDA UDI
SILMET LTD·07290012207624·Dental Amalgam Alloy

GROWTH GUIDANCE PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

ADVANCED GLASS IONOMER (K-130) RESTORATIVE

FDA 510(k)
FDA Class 2 ·Dental

TELIGEN

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 1, 2014

LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

FDA Adverse Event
Malfunction ·REYNOSA MANUFACTURING·Product code FKX·May 14, 2013

ADAPTA SR

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL, INC.·Product code NVZ·June 16, 2011

CAPIOX RX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 26, 2023

CAPIOX RX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 20, 2018

CAPIOX RX OXYGENATOR

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

FDA Adverse Event
Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·January 31, 2024

CAPIOX®RX

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 9, 2024

CAPIOX RX OXYGENATOR

FDA Adverse Event
Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 5, 2018

3.5MM UNIVERSAL DRILL GUIDE

FDA Adverse Event
Malfunction ·SYNTHES HAGENDORF·Product code FZX·September 29, 2017

Siemens LANTIS Oncology Information System Servers; allows the radiation therapist to deliver treatment to patient using the MEVATRON and all available accessories

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·March 25, 2015

Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander The intended use of the linear accelerator is to deliver x-ray radiation for therapeutic treatment of cancer.

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 2, 2014

Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, ORS-300, ORS-301, ORS-320, ORS-321, ORS-325, ORS-330, ORS-331 and ORS-2200. The ORS Fluid Warming and Slush Drapes are individually wrapped and placed in poly-Tyvek pouches with a label insert, then packaged as 24 per case in a labeled corrugated shipper box. Intended for use during various surgeries where warm irrigation, slush and/or cold solution are required.

FDA Enforcement
Class II ·Terminated·Ecolab Inc·September 30, 2015

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

FDA Enforcement
Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015