FORCEMECH INTERNATIONAL LLC.

FDA Device Registration & Listing · Katy, TX, US · Registration 3013934051

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013934051
FEI Number
3013934051
Entity Name
FORCEMECH INTERNATIONAL LLC.
City/State/Country
Katy, TX, US
Establishment Address
4219 Clay Commerce Dr Ste 103, Katy, TX 77449, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Forcemech International LLC. (Owner Number: 10055638)
Owner / Operator Contact Address
4219 Clay Commerce Dr., Suite 103, Katy, TX 77449, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K170787
PMA Number
N/A

All Registered Proprietary Names

Forcemech Liberty, PathMate Forcemech

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2026-01-06
INI Vehicle, Motorized 3-Wheeled Physical Medicine Class 2 890.3800 2026-01-06
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2026-01-06
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2017-08-29
ITI Wheelchair, Powered Physical Medicine Class 2 890.3860 2017-12-12

Official Correspondent

David Ou

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Forcemech International LLC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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

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.
Z-0036-2007 Medline Industries Inc 2
Medline Strider Maxi 3 Scooter; a three wheeled battery operated scooter; manufactured by KYMCO, Kaohsiung, Taiwan for Medline Industries, Inc., One Medline Place, Mundelein, IL 60060 USA; model MDS807600 - red and MDS807600B - blue

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013934051. Last updated year: 2026. Please use registration number 3013934051 when referencing this establishment in official correspondence.
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