BEUDAMED
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    SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-05000-3D2, SDM-05000-3D3, SDM-05000-3DC, SDM-SYS-9000-2D, SDM-SYS-9000-3D.

    FDA Enforcement
    Class II ·Ongoing·Hologic, Inc·May 20, 2026

    Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D SDM-00001-3D SDM-05000-3D3 SDM-05000-2DC SDM-00001-M3D SDM-05000-3DC SDM-SYS-6000-3D SDM-05000-2D3 SDA-SYS-3000-2D SDM-00001 SDM-SYS-9000-2D SDM-00001-M2D 3DM-SYS-STD 3DM-SYS-STD-NS SDM-05000-2AC SDM-05000-2A2 SDA-SYS-3000-3D SDA-SYS-3000-3D-UPS SDM-SYS-6000-3D-HTC SDM-05000-2D2 SDM-05000-3D2 SDM-SYS-6000-2D SDM-SYS-9000-3D

    FDA Enforcement
    Class II ·Ongoing·Hologic, Inc.·March 1, 2023

    PROLENE SUTURE BLUE 4X18"5/0 DA RB-2 +PLG, D7879

    FDA Enforcement
    Class II ·Terminated·Ethicon, Inc.·July 25, 2018

    PROLENE SUTURE BLUE 4X90CM M1.5 USP 4/0 DA RB-1 +P, D5981

    FDA Enforcement
    Class II ·Terminated·Ethicon, Inc.·July 25, 2018

    SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8FS S5 PACK W/CARDIOPLEGIA-3D, (a) REF 044042600 AND (b) REF 044011200, STERILE EO, Rx Only, 1 EA

    FDA Enforcement
    Class II ·Terminated·Sorin Group USA, Inc.·August 9, 2017

    FlexLab (FLX); Version: FLX-217-10;

    FDA Enforcement
    Class II ·Ongoing·Inpeco S.A.·December 3, 2025

    FlexLab (FLX); Version: FLX-217-40;

    FDA Enforcement
    Class II ·Ongoing·Inpeco S.A.·December 3, 2025

    FlexLab (FLX) System. Potassium Test System. in vitro diagnostic

    FDA Enforcement
    Class II ·Ongoing·Inpeco S.A.·October 15, 2025

    FlexLab X (FXX) System. Potassium Test System. in vitro diagnostic

    FDA Enforcement
    Class II ·Ongoing·Inpeco S.A.·October 15, 2025

    ASP BIOTRACE Auto Read 60 Steam BI Process Challenge Device, REF 73135.

    FDA Enforcement
    Class II ·Ongoing·TERRAGENE S.A.·March 5, 2025

    The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for monitoring intracranial ventricular pressure with tunneling (PSO-VT) indicated for use in intraventricular pressure monitoring and cerebrospinal fluid drainage application. Model/Catalog Number: PSO-VT

    FDA Enforcement
    Class II ·Ongoing·Sophysa S.A.·May 22, 2024

    The Sophysa Pressio¿ Ventricular Intracranial Pressure Monitoring Kit monitoring is intended for monitoring intracranial ventricular pressure and temperature with tunneling (PSO-VTT) indicated for use in intraventricular pressure monitoring and cerebrospinal fluid drainage application. Model/Catalog Number: PSO-VTT

    FDA Enforcement
    Class II ·Ongoing·Sophysa S.A.·May 22, 2024

    TDHistology/Cytology Classification name: Calculator/data processing module for clinical use (862.2100). Intended use: Laboratory Information System (L.I.S)

    FDA Enforcement
    Class III ·Terminated·Technidata S.A.·July 24, 2013

    TD-Synergy. Laboratory Information System.

    FDA Enforcement
    Class II ·Terminated·Technidata S.A.·May 29, 2013

    Punch Hair Matic A surgical hair transplant device designed for automation of follicular transplantation.

    FDA Enforcement
    Class II ·Terminated·MEDICAMAT S.A.·March 12, 2014

    FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System

    FDA Enforcement
    Class II ·Terminated·Inpeco S.A.·May 16, 2018

    RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray. Intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts.

    FDA Enforcement
    Class II ·Terminated·Sedecal S.A.·August 26, 2015

    TDWorkstation version 11.01.A or higher. TDWorkstation Evolution. TDWorkstation receives patient results from a connected instrument and sends them to a Laboratory Information System (LIS).

    FDA Enforcement
    Class III ·Terminated·Technidata S.A.·April 9, 2014

    MobileDiagnost wDR motorized portable diagnostic X-ray systems.

    FDA Enforcement
    Class II ·Terminated·Sedecal S.A.·February 11, 2015

    L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for intervertebral body fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the lumbar spine at one or two contiguous levels from L2-S1. DDD is defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies. These DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). L-Varlock Lumbar implants are to be used with autogenous bone graft and implanted via an open posterior approach. L-Varlock Lumbar implant is to be used with supplemental fixation. Patients should have at least six (6) months of non-operative treatment prior to treatment with an intervertebral cage.

    FDA Enforcement
    Class II ·Terminated·Kiscomedica S.A.·March 22, 2017