42 results · 11ms · Sources: EU EUDAMED, US FDA

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CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 m

FDA Recall
Open, Classified ·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·August 18, 2025

CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX only

FDA Recall
Open, Classified ·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·October 16, 2024

EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202

FDA Recall
Open, Classified ·CORNEAT VISION, LTD. 4, Ha-Sheizaf Ra'Anana Israel·Product code QWU·August 18, 2025

Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine (XVS) system, an image-guided navigation system that is designed to assist surgeons in placing pedicle screws accurately, during open or percutaneous computer-assisted spinal surgery.

FDA Recall
Open, Classified ·Augmedics Ltd. 2 Ha-Otsma St Yokneam Illit Northern Israel·Product code OLO·April 14, 2025

DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.

FDA Recall
Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

DigitalDiagnost C90 High Performance, used to acquire, process, store, display and export digital radiographic images.

FDA Recall
Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000

FDA Recall
Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·September 20, 2022

CombiDiagnost R90 R.1.0

FDA Recall
Open, Classified ·Philips North America·Product code JAA·March 3, 2023

CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system

FDA Recall
Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

CombiDiagnost R90; Model Number: 709031;

FDA Recall
Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany·Product code JAA·October 1, 2025

ProxiDiagnost N90. radiography and fluoroscopy system

FDA Recall
Open, Classified ·Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·May 19, 2021

Artis Pheno, Interventional Fluoroscopic X-Ray System, Model No. 10849000

FDA Recall
Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·June 10, 2022

AXIOM Luminos Agile

FDA Recall
Open, Classified ·Siemens Medical Solutions USA, Inc·Product code JAA·December 9, 2022

DigitalDiagnost C90 Release 3, used to acquire, process, store, display and export digital radiographic images.

FDA Recall
Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

CombiDiagnost R90 Software Version R1.0 and R1.1

FDA Recall
Open, Classified ·Philips Medical Systems Gmbh, DMC Development And Manufacturing Ctr. Rontgenstr. 24-26 Hamburg Germany·Product code JAA·July 22, 2020

CombiDiagnost R90 is multi-functional general R/F systems.

FDA Recall
Open, Classified ·Philips Healthcare·Product code JAA·September 22, 2021

ProxiDiagnost N90 R.1.0

FDA Recall
Open, Classified ·Philips North America·Product code JAA·March 3, 2023

CombiDiagnost R90 1.1 (709031)

FDA Recall
Open, Classified ·PHILIPS MEDICAL SYSTEMS·Product code JAA·February 11, 2022

ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system

FDA Recall
Open, Classified ·Philips North America Llc·Product code JAA·September 21, 2023

Azurion R3.0. Model Number 722234. Commercial Name: Azurion 7 M20. INTERVENTIONAL FLUOROSCOPIC XRAY SYSTEM

FDA Recall
Open, Classified ·Philips North America·Product code JAA·October 27, 2025