Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9615246

FEI Number

3006662254

Entity Name

TOLLOS MANUFACTURING

City/State/Country

Barrie Ontario, CA

Establishment Address

75 Dyment Rd, Barrie Ontario L4N 3H6, CA

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Complaint File Establishment per 21 CFR 820.198

Owner / Operator

2437090 Ontario Ltd DBA Tollos Manufacturing (Owner Number: 10055730)

Owner / Operator Contact Address

75 Dyment Rd, Barrie, CA-ON L4N 3H6, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Ultralift Mobile Lift UltraMove Medical Assisting Device Cirrus Fix Ceiling Lift Pinnacle Fix Ceiling Lift Stratus II Portable Ceiling Lift Titan Mobile Lift Steady Aid Medical Assisting Device Reusable Dual Turner Harness Reusable Repositioning Sling Reusable Walking Harness Reusable Steady Aid Harness Reusable Multi-Purpose Band Harness Reusable Steady Aid Elite Harness Single Use Repositioning Sling Single Use Combi Sling Single Use Steady Aid Harness Reusable Hygiene Elite Sling Single Use Long Seat Sling Reusable Long Seat Sling Reusable Combi Sling Single Use Multi-Purpose Band Harness

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSA	Lift, Patient, Non-Ac-Powered	General Hospital	Class 1	880.5510	2017-09-27
IKX	Aid, Transfer	Physical Medicine	Class 1	890.5050	2024-12-27

Official Correspondent

Diego Cristancho

US Agent Details

Diego Cristancho Business: 2437090 Ontario Ltd DBA Tollos Manufacturing Email: dcristancho@tollos.com Phone: (443) 8365920

Related Public Records

Same Entity

2437090 Ontario Ltd DBA Tollos Manufacturing

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-0013-2018	Handicare Usa Inc	1	PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
Z-0014-2018	Handicare AB Maskinvagen	1	Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

Similar Registrations

Registration Number	Establishment Name	Location
3027517735	LIANJIA (ZHONGSHAN) GONGMAO CO.LTD	Zhongshan Guangdong, CN
3008406502	Tollos	Sioux Falls, SD, US
3004648937	Winncare Nordic ApS	KORSOR Sjalland, DK
3013528441	Green Source Technology (Hebei) Inc.	Langfang City Hebei, CN
3042255028	SUSHI INTELLIGENT TECHNOLOGY (CHANGZHOU) CO.,LTD	Changzhou Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615246. Last updated year: 2026. Please use registration number 9615246 when referencing this establishment in official correspondence.