1767388 Ontario Inc
FDA registration: United States Last updated 25 May 2026
- Devices
- 13
- Registries
- GUDID
- FDA recalls
- 0
Catalogue
What 1767388 Ontario Inc makes
The company manufactures basic electric hospital beds, including the Spirit Select model, designed for patient care in clinical settings.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Frequently asked questions
What types of medical devices does 1767388 Ontario Inc manufacture?
1767388 Ontario Inc specializes in basic electric hospital beds, such as the Spirit Select model. These devices are engineered for patient care in clinical environments, providing adjustable support and mobility for healthcare settings.
Where is 1767388 Ontario Inc based?
The company is headquartered in the United States. This location allows it to comply with U.S. regulatory standards, including those governing medical devices like electric hospital beds.
How are the devices manufactured by 1767388 Ontario Inc classified under FDA regulations?
The company’s devices, including basic electric hospital beds like the Spirit Select, fall under Class II classification by the FDA. This classification typically applies to devices with a moderate level of risk, requiring special controls beyond general controls to ensure safety and effectiveness.
Are the devices from 1767388 Ontario Inc listed in any regulatory databases?
Yes, the company’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices like electric hospital beds to ensure transparency and traceability in the healthcare supply chain.
Information
- FDA registration
- United States
- DUNS number
- 253655708