Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1221084

FEI Number

1221084

Entity Name

PERMOBIL, INC.

City/State/Country

LEBANON, TN, US

Establishment Address

300 Duke Dr, LEBANON, TN 37090, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

PERMOBIL INC (Owner Number: 8030931)

Owner / Operator Contact Address

300 DUKE DR, Lebanon, TN 37090, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K041219

PMA Number

N/A

All Registered Proprietary Names

F3 Corpus STELLAR GLT. STELLAR IMPACT, STELLAR HD, STELLAR GL BENTLEY, BENTLEY LT-R, BENTLEY LT FUZE T50N, FUZE JR, FUZE M50, FUZE T50 M300 PS Junior TiLite X PDG Mobiity components Lifestand Components Permobil wheelchair components Smart Drive components F5 Corpus ECLIPSE K450 K300 PS Junior

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2015-04-14
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2025-11-24
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2025-11-24
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2025-11-24
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2013-11-27
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2024-07-16
KNN	Components, Wheelchair	Physical Medicine	Class 1	890.3920	2011-04-28
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2015-04-14
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2020-06-12
IOR	Wheelchair, Mechanical	Physical Medicine	Class 1	890.3850	2025-11-24
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2013-11-27
ITI	Wheelchair, Powered	Physical Medicine	Class 2	890.3860	2006-05-17

Official Correspondent

Ivan Fernandez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PERMOBIL 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
8030931	PERMOBIL AB	Sundsvall Vasternorrland, SE

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K853594	Vessa , Ltd.	VESSA FLIVVA	1985-09-24
K142783	Heartway Medical Products Co., Ltd.	HEARTWAY Electrically Powered Wheelchair P27	2015-06-12
K935211	Brookefield Hunter, Inc.	WALK N CHAIR	1994-02-02
K832685	Health America	WHEELCHAIR-VARIOUS MODELS	1983-09-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
Z-0006-2018	Permobil, Ab Arvaltsvagen 10	2	Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Z-0039-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624EZ Power Wheel Chairs with internally threaded wheel mount motors.
Z-0040-2007	Eagle Parts and Products	2	Eagle Parts and Products Model 624Mini Power Wheel Chairs with internally threaded wheel mount motors.

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3002667030	TUNG KENG ENTERPRISE CO., LTD.	Taichung City, TW
3043165991	HEBEI DANSONG MEDICAL TECHNOLOGY CO., LTD.	SHIJIAZHUANG Hebei, CN
3036988603	SHENZHEN YATTLL INDUSTRY CO., LTD	Shenzhen Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1221084. Last updated year: 2026. Please use registration number 1221084 when referencing this establishment in official correspondence.