49 results · 7ms · Sources: EU EUDAMED, US FDA

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Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050

FDA Enforcement
Class II ·Terminated·Stryker GmbH·January 15, 2020

Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone.

FDA Enforcement
Class II ·Terminated·Zimmer Gmbh·October 21, 2015

LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert

FDA Enforcement
Class II ·Ongoing·CORENTEC CO., LTD·June 12, 2024

Zimmer Natural Nail -ZNN Cephalomedullary Short Nail 11.5 mm X 21.5 cm 125 CCD Left Ti-6Al-4V Alloy- intended for temporary fracture fixation and stabilization of the bone Item Number: 47-2493-211-11

FDA Enforcement
Class II ·Terminated·Zimmer GmbH·June 9, 2021

Zimmer Natural Nail- ZNN Cephalomedullary Short Nail 11.5 mm X 21.5 cm 130 CCD Left Ti-6Al-4V Alloy-is intended for temporary fracture fixation and stabilization of the bone Item Number: 47-2493-213-11

FDA Enforcement
Class II ·Terminated·Zimmer GmbH·June 9, 2021

Cephalomedullary Nail (CMN), Various sizes, Item Nos. 47249318009 47249318010 47249318011 47249318013 47249318014 47249318109 47249318110 47249318111 47249318113 47249318114 47249318209 47249318210 47249318211 47249318213 47249318214 47249318309 47249318310 47249318311 47249318313 47249318314 47249321010 47249321011 47249321013 47249321014 47249321110 47249321111 47249321113 47249321114 47249321210 47249321211 47249321213 47249321214 47249321310 47249321311 47249321313 47249321314 47249321410 47249321411 47249321413 47249321414 47249321510 47249321511 47249321513 47249321514 47249330010 47249330011 47249330013 47249330110 47249330111 47249330113 47249330210 47249330211 47249330213 47249330310 47249330311 47249330313 47249330410 47249330411 47249330413 47249330510 47249330511 47249330513 47249332010 47249332011 47249332013 47249332110 47249332111 47249332113 47249332210 47249332211 47249332213 47249332310 47249332311 47249332313 47249332410 47249332411 47249332413 47249332510 47249332511 47249332513 47249334010 47249334011 47249334013 47249334110 47249334111 47249334113 47249334210 47249334211 47249334213 47249334310 47249334311 47249334313 47249334410 47249334411 47249334413 47249334510 47249334511 47249334513 47249336010 47249336011 47249336013 47249336110 47249336111 47249336113 47249336210 47249336211 47249336213 47249336310 47249336311 47249336313 47249336410 47249336411 47249336413 47249336510 47249336511 47249336513 47249338010 47249338011 47249338013 47249338110 47249338111 47249338113 47249338210 47249338211 47249338213 47249338310 47249338311 47249338313 47249338410 47249338411 47249338413 47249338510 47249338511 47249338513 47249340010 47249340011 47249340013 47249340110 47249340111 47249340113 47249340210 47249340211 47249340213 47249340310 47249340311 47249340313 47249340410 47249340411 47249340413 47249340510 47249340511 47249340513 47249342010 47249342011 47249342013 47249342110 47249342111 47249342113 47249342210 47249342211 47249342213 47249342310 47249342311 47249342313 47249342410 47249342411 47249342413 47249342510 47249342511 47249342513 47249344010 47249344011 47249344013 47249344110 47249344111 47249344113 47249344210 47249344211 47249344213 47249344310 47249344311 47249344313 47249344410 47249344411 47249344413 47249344510 47249344511 47249344513 47249346010 47249346011 47249346013 47249346110 47249346111 47249346113 47249346210 47249346211 47249346213 47249346310 47249346311 47249346313 47249346410 47249346411 47249346413 47249346510 47249346511 47249346513 47249348010 47249348011 47249348013 47249348110 47249348111 47249348113 47249348210 47249348211 47249348213 47249348310 47249348311 47249348313 47249348410 47249348411 47249348413 47249348510 47249348511 47249348513

FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·November 13, 2019

ICN TRANSDUCER KIT W/30ML FLUSH DEVICE FOR STANFORD UNIV. HOSP., Item No. 46065-64 The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into electrical currents that can be input into a compatible pressure monitor. The SafeSet Reservoir system is a blood sampling system assembled directly to the patient monitoring line (Transpac units). The SafeSet reservoir is used on patients where periodic blood sampling is required.

FDA Enforcement
Class II ·Terminated·ICU Medical, Inc.·November 23, 2016

IBA Proton Therapy System - PROTEUS 235

FDA Enforcement
Class II ·Ongoing·Ion Beam Applications S.A.·March 18, 2026

IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions, PTS-11 versions, and PTS-12 versions

FDA Enforcement
Class II ·Ongoing·Ion Beam Applications S.A.·September 18, 2024

IBA Proton Therapy System - PROTEUS 235 - Designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

FDA Enforcement
Class II ·Ongoing·Ion Beam Applications S.A.·June 12, 2024

Proteus 235 Proton Therapy System Legacy Software version 7.2.7 and higher, models 110, 112, 113, and 116. Proton therapy

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·April 30, 2014

Proton therapy system -Proteus 235 aka Proteus Plus. A medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·May 24, 2017

Proteus 235, Proton Therapy System

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·April 26, 2017

Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·July 18, 2018

Proteus 235, Universal Nozzle with snout 300x400; PBS dedicated nozzle with snout XL Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatment room dedicated to the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation localized to the head and neck.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·July 25, 2018

Proteus 235, Pencil Beam Scanning version PTS-6.4.11.X The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatment room dedicated to the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation localized to the head and neck.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·March 14, 2018

Proteus ONE and Proteus Plus

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·June 20, 2018

adaPT insight (12C), v1.3.2, PAT.109 (US), Treatment room 4: I2C is used with a charged particle or photon radiation therapy system for localization of the patient position with respect to the therapy equipment and to provide correction feedback to the radiation therapy device.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·December 31, 2014

Proteus 235 Proton Therapy System for cancer treatment.

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·November 5, 2014

Proteus 235

FDA Enforcement
Class II ·Terminated·Ion Beam Applications S.A.·April 5, 2017