BEUDAMED
    17 results · 8ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: Class Ii × Regulation: Us FDA × Clear all

    AUTO REF/KERATOMETER ARK-1s

    FDA Enforcement
    Class II ·Terminated·Nidek Inc.·April 18, 2018

    Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) allows clinicians to drill through a surgical guide to create an osteotomy for implant placement with the precision and accuracy as designed with treatment planning software. The G-HK consists of 4 guide handles with inserts attached on each end. Each insert has an opening that matches the diameter of our surgical drills. The insert portion of the guide handle fits intimately into the guide sleeve that is embedded into a surgical guide.

    FDA Enforcement
    Class II ·Terminated·Implant Direct Sybron Manufacturing, LLC·December 27, 2017

    Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows clinicians to drill through a surgical guide to create an osteotomy for implant placement with the precision and accuracy as designed with treatment planning software. The G-HK consist of 4 guide handles with inserts attached on each end. Each insert has an opening that matches the diameter of our surgical drills. The insert portion of the guide handle fits intimately into the guide sleeve that is embedded into a surgical guide.

    FDA Enforcement
    Class II ·Terminated·Implant Direct Sybron Manufacturing, LLC·September 20, 2017

    GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1

    FDA Enforcement
    Class II ·Terminated·Medacta Usa Inc·June 15, 2022

    GMK Hinge knee prosthesis; Model Number: 02.09.TA410; Orthopedics and Orthopedic Surgery

    FDA Enforcement
    Class II ·Terminated·Medacta Usa·November 25, 2015

    Medacta GMK HINGE, Tibial Insert Fixed, SIZE 2, HEIGHT 23 mm, REF 02.09.0223H, STERILE EO

    FDA Enforcement
    Class II ·Terminated·Medacta Usa Inc·July 12, 2017

    The GMK knee system: designed for cemented use in total knee arthroplasty. Sphere and Primary Inserts with part number ranges: 02.12.0110FL - 02.12.0620FL; 02.12.0110FR - 02.12.0620FR; 02.07.0110PSF - 02.07.0620PSF

    FDA Enforcement
    Class II ·Terminated·Medacta Usa Inc·December 27, 2017

    GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement.

    FDA Enforcement
    Class II ·Terminated·Medacta Usa·November 19, 2014

    GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    FDA Enforcement
    Class II ·Ongoing·GE Medical Systems Information Technologies Inc·June 3, 2026

    GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

    FDA Enforcement
    Class II ·Ongoing·GE Medical Systems Information Technologies Inc·June 3, 2026

    ClubMax Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Atom Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Maxim Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Spectrum Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Burstberry Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Logolas Laser Projection Series

    FDA Enforcement
    Class II ·Ongoing·Gk Photonics Inc·August 14, 2019

    Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a reusable surgical instrument designed to limit the magnitude of applied (input) torque transferred to an external (output) device or fastener in the clockwise direction. The device is a non-adjustable mechanical click style hand torque tool which presents an audible and tactile click when the maximum desired torque is reached.

    FDA Enforcement
    Class II ·Terminated·Bradshaw Medical Inc.·May 18, 2016