VELA VERMUND LARSEN A/S

FDA Device Registration & Listing · Aalborg SV Nordjylland, DK · Registration 3004132709

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
3004132709
FEI Number
3004132709
Entity Name
VELA VERMUND LARSEN A/S
City/State/Country
Aalborg SV Nordjylland, DK
Establishment Address
Goteborgvej 12, Aalborg SV Nordjylland 9200, DK
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
VELA Vermund Larsen A/S (Owner Number: 10031625)
Owner / Operator Contact Address
Goteborgvej 12, Aalborg SV, DK-81 9200, DK
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VELA Latin, VELA Tango VELA Tango 700E with Power Wheels VELA Meywalk 4 VELA Meywalk 2000 VELA Miniwalk VELA Hip Hop 100; VELA Rumba; VELA Salsa; VELA Samba INN

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
INM Chair, With Casters Physical Medicine Class 1 890.3100 2010-02-22
INO Chair, Positioning, Electric Physical Medicine Class 2 890.3110 2024-08-20
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2024-08-20
INN Chair, Adjustable, Mechanical Physical Medicine Class 1 890.3100 2011-12-16

Official Correspondent

Mathias Jungersen

US Agent Details

Robert Bard Business: HealthCare Technologies Consultants Email: rbard@reglaw.net Phone: (248) 5735040

Related Public Records

Same Entity

VELA Vermund Larsen A/S
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0011-2015 Nemschoff Chairs, Inc. 909 N 8th St 2218 Julson Ct Sheboygan WI 53081-4056 1
Nemschooff, Model Numbers - Serenity II:790-12, Serenity III: 791-12, Serenity III Exam: 791-12E, and Serenity IIS: 792-12. Designed to provide patient comfort during patient treatment sessions. The chair may include a manual control reclining mechanism. Customer configurable models are also available. The Serenity III Exam 791-12E was discontinued 11/1/2010.
Z-0031-2013 Winco Mfg., LLC 1
Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No. 536A-101475***" Literature: "***Caremor Cliner 5351/5361***Winco***ISO 9001-2008 Certified***Our most comfortable and versatile recliner***Ease of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.***KEY FEATURE'S***Infinite positioning back***Padded armrests w/arm guard***Webbed elastic suspension back and seat***Removable side panels**Continuous seat & legrest cushion***5351 w/tray***5361 w/out tray***1.800.237.3377***5516 SW 1st Lane***Ocala, Florida 34474***www.wincomfg.com***Proudly Made in the USA***" Patient recliner chair
Z-0032-2013 Winco Mfg., LLC 1
Caremor Cliner is labeled in part: "***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 535 Serial No. 535A-104522***" Literature: "***Caremor Cliner 5351/5361***Winco***ISO 9001-2008 Certified***Our most comfortable and versatile recliner***Ease of operation, outstanding durability, and exceptional value have made this one of our bestselling recliners. The Caremor Cliner provides patient comfort and support as well as user friendly features.***KEY FEATURE'S***Infinite positioning back***Padded armrests w/arm guard***Webbed elastic suspension back and seat***Removable side panels**Continuous seat & legrest cushion***5351 w/tray***5361 w/out tray***1.800.237.3377***5516 SW 1st Lane***Ocala, Florida 34474***www.wincomfg.com***Proudly Made in the USA***" Patient recliner chair

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004132709. Last updated year: 2026. Please use registration number 3004132709 when referencing this establishment in official correspondence.
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