BEUDAMED
    14 results · 28ms · Sources: EU EUDAMED, US FDA

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    BLOM-SINGER INDWELLING LOW PRESSURE VOICE PROSTHES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Ophthalmic Spatula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668102336·WHEELER SPATULA DOUBLE-END

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194482·Interbody, 9mm x 32mm x 12mm, 0 deg

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111017·SILICONE MAT FOR INSTRUMENT CADDY

    General

    FDA UDI
    Seaspine Orthopedics Corporation·10889981088002·Plunger

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202477·Interbody, 9mm x 32mm x 12mm, 0 deg

    WTF SECURA SYRINGE AND NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROMINJET PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    IMPELLA CP

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·December 30, 2025

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LIX·April 3, 2014

    ACCU-CHEK PERFORMA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS INC.·Product code LZG·January 18, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 17, 2010

    Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 178360 178361 178362 178363 178364 178365 178366 178367 178368 178369 178370 178371 178372 178373 178464 178472 178480 178488 178496 178504 178575 178576 178577 178578 178579 178580 178730 178731 178732 178733 178734 178735 178354S 178754 178755 178756 178757 178758 178759 Product Usage: 1) Correction of revision of unsuccessful osteotomy, arthrodesis or previous joint replacement 2) Tumor resections 3) Revision of previously failed total joint arthroplasty 4) Trauma The ComPreSs Distal Femoral Replacement System is intended for uncemented use.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019

    OPTETRAK LOGIC Polyethylene Tibial Inserts, labeled as the following: a. OPTETRAK Logic PS Tibial Inserts, Product Line 02-012-35-XXXX; b. OPTETRAK Logic PSC Tibial Inserts, Product Line 02-012-44-XXXX; c. OPTETRAK Logic CR Tibial Inserts, Product Line 02-012-47-XXXX; d. OPTETRAK Logic CR Slope + Tibial Inserts, Product Line 02-012-48-XXXX; e. OPTETRAK Logic CR Slope ++ Tibial Inserts, Product Line 02-012-49-XXXX; f. OPTETRAK Logic CRC Tibial Inserts, Product Line 02-012-51-XXXX; g. OPTETRAK Logic CC Tibial Inserts, Product Line 02-012-65-XXXX; Affected 510(k) numbers include: K033883, K132161, K093360, K110547, K111400, K121307, K123342, K150890. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021