Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003124453

FEI Number

3003124453

Entity Name

Acorn Stairlifts, Inc

City/State/Country

Belle Isle, FL, US

Establishment Address

7001 Lake Ellenor Dr, Belle Isle, FL 32809, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Acorn Stairlifts Inc (Owner Number: 10046507)

Owner / Operator Contact Address

7001 Lake Ellenor Drive, Orlando, FL 32809, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Acorn 120 Stairlift Acorn 120 Outdoor Stairlift Brooks 120 Stairlift Brooks 120 Superglide Stairlift Acorn Outdoor Stairlift Acorn 120 Slimline Stairlift Brooks Outdoor Stairlift Acorn 120 Superglide Stairlift Brooks 120 Slimline Stairlift Acorn 80 Stairlift Acorn 130 Stairlift Brooks 130 Stairlift Acorn 180 Stairlift

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PCD	Powered Stairway Chair Lift	Physical Medicine	Class 2	890.5150	2014-03-31

Official Correspondent

Shawn Herbst

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Acorn Stairlifts Inc

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3033915638	ACORN STAIRLIFTS INC	Lorain, OH, US

Similar Registrations

Registration Number	Establishment Name	Location
3006310491	ACORN MOBILITY SERVICES LTD	Keighley Bradford, GB
3004781011	Harmar Mobility, LLC	Sarasota, FL, US
3011268530	Savaria Lifts (UK) Ltd.	Kingswinford Dudley, GB
3026960440	DEVI-STAIRLIFTS BV	Opmeer Noord-Holland, NL
3031806435	STAIRASSIST WALKER, INC.	Scituate, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003124453. Last updated year: 2026. Please use registration number 3003124453 when referencing this establishment in official correspondence.