BEUDAMED
    27 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    LINK® SP-CL® Hip System PoroLink® (microporous) and HX® (CaP) coated & LINK® LCU® Hip System PoroLink® (microporous) and HX® (CaP) coated

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741618400·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674161840060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1618400·16mm H x 18mm W x 40mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16184080·16mm H x 18mm W x 40mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X161840120·16mm H x 18mm W x 40mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L161840120·16mm H x 18mm W x 40mm L XLIF Trial 12 degree L...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916121822·ZEUS®-L Implant, 16 x 18 x 40mm, Lordotic

    Zavation

    FDA UDI
    Zavation LLC·00842166150157·16x18x40mm, 6°, MILC

    Zavation

    FDA UDI
    Zavation LLC·00842166149403·16x18x40mm, 0°, MILC

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916121839·ZEUS®-L Implant, 16 x 18 x 40mm, Parallel

    EMERGE FRACTIONAL LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929037010·Corpectomy, 16Dx18Wx40H 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066010·Corpectomy, 16Dx18Wx40H 0°

    GMK-HINGE FIXED TIBIAL INSERT SIZE 3/14MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·September 7, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    SECURA VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·October 10, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·June 11, 2013