Skip to content

MGsolutions Inc.

South Korea KR-MF-000051033 Last updated 23 Oct 2026

Is this your brand? Sign in to claim this brand

Devices
1
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue1

Authorised representatives

What MGsolutions Inc. makes

MGsolutions Inc. manufactures the Moti Physio Med, a device designed for physiotherapy applications, likely targeting musculoskeletal rehabilitation or mobility support.

The Moti Physio Med is classified as a Class I medical device and is registered in the EU’s eudamed database. The company is based in South Korea.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does MGsolutions Inc. manufacture?

MGsolutions Inc. specializes in physiotherapy devices. Their primary product, the Moti Physio Med, is designed for musculoskeletal rehabilitation or mobility support, helping patients recover or maintain function through targeted therapy.

Where is MGsolutions Inc. based?

MGsolutions Inc. is headquartered in South Korea, where it develops and manufactures its medical devices, including the Moti Physio Med.

Which regulatory registries list MGsolutions Inc.’s devices?

The Moti Physio Med is listed in the EU’s eudamed database, which serves as a central registry for medical devices authorized in the European Economic Area. This inclusion indicates compliance with EU regulatory requirements for Class I devices.

How are MGsolutions Inc.’s devices classified under medical device regulations?

The Moti Physio Med falls under Class I classification, which typically applies to low-risk devices like bandages, gloves, or basic rehabilitation tools. This classification is determined by factors such as the device’s intended use, risk profile, and interaction with the body, ensuring it meets the minimum regulatory standards for safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
South Korea
Address
1F, 5F, 10, Donggyo-ro 23-gil, Seoul, South Korea
PRRC contact
Jinyoung Lee
EUDAMED SRN
KR-MF-000051033
FDA FEI number
3042197714