BEUDAMED
    22 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 ×

    MyDay (stenfilcon A) Soft (Hydrophilic) Daily Disposable Contact Lens, Avaira Vitality (fanfilcon A) Soft (Hydrophilic) Contact Lens

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MOTOCLIP

    FDA Adverse Event
    Malfunction ·CROSSROADS EXTREMITY SYSTEMS·Product code JDR·September 29, 2022

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112564·BARRON CORNEAL PUNCH 6.0MM

    Symmetry Davis

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482059074·Symmetry® Spatula; Davis Brain; Malleable; 7/8 ...

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869604253·MOSS Ti Rod, Ø5.5x70mm, straight

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869621304·MOSS VRS Ti rod, Ø5.5x70mm, straight

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197474436·Beckmann adenoid curette Fig. 7...

    RIVA Posterior Fixation System

    FDA UDI
    XENIX MEDICAL LLC·00840493415703·Closed Lateral Connector, 70mm

    SYNTHES VARIABLE ANGLE LCP ELBOW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002

    FDA 510(k)
    FDA Class 2 ·Dental

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962113660·DAVIS BRAIN SPATULA, 7/8"X7"

    Widex

    FDA UDI
    Widex A/S·05706069794571·Widex BEYOND B-F2 (Copper brown ) 220, Telecoil...

    NA

    FDA UDI
    Zimmer, Inc.·00889024187788·

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 31, 2008

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FRN·August 12, 2011

    ATLAS II VR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2013

    Trach-Eze Closed Suction System Endotracheal Start Kit *** 16F *** REF 220070 *** Catheter Length: 571 mm *** STERILE ***.

    FDA Recall
    Terminated ·Sorenson Medical, Inc.·Product code BSY·November 25, 2002

    RESTYLANE DEFYNE

    FDA Adverse Event
    Injury ·Q-MED·Product code LMH·June 15, 2023

    SLIDING MECHANISM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·January 9, 2024

    bvi Beaver Safety Sideport Knife: (a) 1.0mm, 45o, REF 378210 (b) 1.2mm, 45o, REF 378212 (c) 115mm, 45o, REF 378231 Product Usage: Specialty blades and knives are used for stab and cut incisions in ophthalmic, ENT and other surgical applications.

    FDA Enforcement
    Class II ·Terminated·Beaver-Visitec International Inc.·February 7, 2018