BEUDAMED
    124 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL-KNEE(R) AND NATURAL KNEE(R)II W/CSTI(TM)

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL-KNEE(R) WITH CSTI(TM)

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL-KNEE(R) WITH CSTI(TM)

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL-KNEE AND NATURAL-KNEE II

    Prosthesis, Knee, Patello/Femorotibial, Unconstrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

    FDA Pre-Market Approval
    FDA Class 3 ·NATURAL KNEE & NATURAL KNEE II

    XLIF

    FDA UDI
    Nuvasive, Inc.·00887517415837·XLIF Slap Hammer

    SURGISTAR

    FDA UDI
    SURGISTAR, INC.·00878799004116·

    NA

    FDA UDI
    Stryker GmbH·07613252445814·

    Doran Scales

    FDA UDI
    DORAN SCALES, INC.·00850013361250·Diaper and Specimen Scale 2x0.0002lb (1000x0.1g)

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G5869400020·arthroscopic iron punch, w/ ratchet, working le...

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G586OP7164370·tennant titanium tying forceps, w/ guide pin & ...

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G586UR6213360·ochsner (fenger) gall stone probe, flexible, 15...

    V-Go Disposable Insulin Delivery

    FDA UDI
    MANNKIND CORPORATION·00385609400025·30 Units/24 hour basal rate and up to 36 Units ...

    NA

    FDA UDI
    Zimmer, Inc.·00889024065567·

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·ENDOLOGIX POWERLINK SYSTEM

    Stent, Superficial Femoral Artery

    FDA Pre-Market Approval
    FDA Class 3 ·MISAGO PERIPHERAL SELF-EXPANDING STENT SYSTEM

    IFACTOR

    FDA Adverse Event
    Injury ·CERAPEDICS·Product code NOX·September 30, 2025

    AFX

    FDA Adverse Event
    Injury ·ENDOLOGIX INC.·Product code MIH·March 1, 2017

    ADULT DUAL-HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·December 28, 2010

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO MEDICAL EQUIPMENT·Product code IOR·February 1, 2013