Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1319061

FEI Number

1319061

Entity Name

Community Products, LLC

City/State/Country

RIFTON, NY, US

Establishment Address

103 Woodcrest Drive, RIFTON, NY 12471, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Community Products, LLC dba Rifton Equipment (Owner Number: 1319061)

Owner / Operator Contact Address

103 Woodcrest Drive, Rifton, NY 12471, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

E-Pacer Support Station Stander Adaptive Desk Pacer Tricycles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2007-02-21
INW	Table, Mechanical	Physical Medicine	Class 1	890.3750	2007-02-21
ITJ	Walker, Mechanical	Physical Medicine	Class 1	890.3825	2007-02-21
ION	Exerciser, Non-Measuring	Physical Medicine	Class 1	890.5370	2002-03-22

Official Correspondent

Travis Scott

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Community Products, LLC dba Rifton Equipment

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1319558	COMMUNITY PRODUCTS, LLC	ELKA PARK, NY, US
3010761454	Community Products, LLC	Farmington, PA, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1319061. Last updated year: 2026. Please use registration number 1319061 when referencing this establishment in official correspondence.