ANATOMIC SITT I NORRKOPING AKTIEBOLAG

FDA Device Registration & Listing · Norrkoping Ostergotland, SE · Registration 3015218514

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
3015218514
FEI Number
3015218514
Entity Name
ANATOMIC SITT I NORRKOPING AKTIEBOLAG
City/State/Country
Norrkoping Ostergotland, SE
Establishment Address
Terminalgatan 1, Norrkoping Ostergotland 60361, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Anatomic Sitt i Norrkoping Aktiebolag (Owner Number: 10057327)
Owner / Operator Contact Address
Terminalgatan 1, Norrkoping, SE-E 60361, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNO Accessories, Wheelchair Physical Medicine Class 1 890.3910 2019-02-14
IMM Footrest, Wheelchair Physical Medicine Class 1 890.3920 2019-02-14
INM Chair, With Casters Physical Medicine Class 1 890.3100 2019-02-14
IQB Belt, Wheelchair Physical Medicine Class 1 890.3920 2019-02-14
IML Armrest, Wheelchair Physical Medicine Class 1 890.3920 2019-02-14

Official Correspondent

Pontus Lindvall

US Agent Details

Susan Matuska Business: Clarke Health Care Products Email: smatuska@clarkehealthcare.com Phone: (724) 6952122

Related Public Records

Same Entity

Anatomic Sitt i Norrkoping Aktiebolag
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 3015218514. Last updated year: 2026. Please use registration number 3015218514 when referencing this establishment in official correspondence.
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