BEUDAMED
    27 results · 46ms · 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.

    Community Products, LLC

    FDA registration
    Community Products, LLC·4 products·🇺🇸 United States

    COMMUNITY PRODUCTS, LLC

    FDA registration
    COMMUNITY PRODUCTS, LLC·3 products·🇺🇸 United States

    Community Products, LLC

    FDA registration
    Community Products, LLC·3 products·🇺🇸 United States

    COMMUNITY MEDICAL PRODUCTS LLC

    FDA registration
    COMMUNITY MEDICAL PRODUCTS LLC·2 products·🇺🇸 United States

    RIFTON

    FDA Adverse Event
    Other ·COMMUNITY PRODUCTS LLC·Product code ION·September 9, 2011

    AQUACEL FOAM

    FDA Adverse Event
    Injury ·CONVATEC INC·Product code NAC·October 6, 2014

    SUPARTZ FX

    FDA Adverse Event
    Injury ·SEIKAGAKU CORPORATION·Product code MOZ·January 11, 2018

    Rifton E-Pacer, SKU K660, powered lift device

    FDA Recall
    Terminated ·Community Products, LLC·Product code FSA·March 21, 2019

    Toddler Chair Hip Strap (Belt). The hip belt is made with nylon webbing and a plastic buckle. 510(k) exempt, Medical Device Listing # R061877. The product is used as a hip strap chair for children.

    FDA Recall
    Terminated ·Community Products, LLC·Product code INN·September 12, 2008

    Rifton TRAM Standard Base, SKU K310, powered lift device

    FDA Recall
    Terminated ·Community Products, LLC·Product code FSA·March 21, 2019

    Rifton TRAM Low Base, SKU K320, powered lift device

    FDA Recall
    Terminated ·Community Products, LLC·Product code FSA·March 21, 2019

    Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds.

    FDA Recall
    Open, Classified ·Community Products, LLC·Product code FSA·December 18, 2025

    Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.

    FDA Recall
    Open, Classified ·Community Products, LLC·Product code FSA·December 18, 2025

    Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.

    FDA Recall
    Open, Classified ·Community Products, LLC·Product code FSA·December 18, 2025

    Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.

    FDA Enforcement
    Class II ·Ongoing·Community Products, LLC·January 28, 2026

    Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.

    FDA Enforcement
    Class II ·Ongoing·Community Products, LLC·January 28, 2026

    Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds.

    FDA Enforcement
    Class II ·Ongoing·Community Products, LLC·January 28, 2026

    Rifton TRAM Low Base, SKU K320, powered lift device

    FDA Enforcement
    Class II ·Terminated·Community Products, LLC·October 30, 2019

    Rifton TRAM Standard Base, SKU K310, powered lift device

    FDA Enforcement
    Class II ·Terminated·Community Products, LLC·October 30, 2019

    Rifton E-Pacer, SKU K660, powered lift device

    FDA Enforcement
    Class II ·Terminated·Community Products, LLC·October 30, 2019