BEUDAMED
    63 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 ×

    POLY Q (GARANT L, PENTA M, PENTA H)

    FDA 510(k)
    FDA Class 2 ·Dental

    HybenX

    FDA UDI
    BICON, LLC·00813110027337·HybenX OTD Syringe (2-Pack)

    Scott's Select Mirror Handle Cone Socket Octagonal

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77810320011·Octagonal cylindrical instrument handle to be u...

    EZflow

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043320013·

    MIS Bunion Accessory Kit (47-0028-S)

    FDA UDI
    Eca Medical Instruments·00850078396013·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07310K0120010·Screwdriver, Tower Tab, Cannulated

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0120010·Draw Rod, Universal Assembly

    K032008

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007

    Kaliec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0300010·Probe, 1.75" Egg, Steffee Long Str Imp Crimson

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0380010·Handle, AO, External, Non-ratcheting

    MONTANE DOLOMITES E-S2.F0 [SZER 69 CM ]

    FDA UDI
    MEDEN INMED SP Z O O·05903684802326·The MONTANE treatment table is a treatment tabl...

    TI-SCREW BUTTRESS THREAD

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code HSB·June 21, 2001

    BREEZE SLEEPGEAR WITH DREAMSEAL

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SMARTSCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERI-STRIPS DRY

    FDA Adverse Event
    Other ·BIO-VASCULAR·Product code FTL·June 1, 2001

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·April 26, 2001

    VASOSEAL ES

    FDA Adverse Event
    Injury ·DATASCOPE CORP./COLLAGEN PRODUCTS·Product code MGB·April 4, 2001

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·April 6, 2001

    VORTEX PORT-AC WITH KIT

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 30, 2001

    *

    FDA Adverse Event
    Other ·JARIT·Product code GZT·August 9, 2001