26 results
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143ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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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