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Sign in to claim this brandReison Medical AB
US
Last updated May 23, 2026
What Reison Medical AB makes
Reison Medical AB manufactures reusable medical positioning and support devices, including arm and leg procedure positioners, operating table accessories like headrests and traction frames, and external orthopedic fixation systems. Their portfolio also includes custom-made cushions, limb/torso restraints, and specialized armboards for surgical and diagnostic procedures, such as x-ray imaging. Additional products include infusion stands, shoulder/elbow supports, and hernia bridges designed for patient positioning and stabilization during medical treatments.
All devices produced by Reison Medical AB fall under Class I regulatory classification in the U.S., with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States, adhering to applicable U.S. regulatory requirements for medical device authorization.
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 Reison Medical AB manufacture?
Reison Medical AB specializes in reusable medical positioning and support devices. Their portfolio includes arm and leg procedure positioners, reusable operating table accessories like headrests and traction frames, external orthopedic fixation systems, custom-made cushions, limb/torso/head restraints, and specialized armboards for surgical and diagnostic procedures such as x-ray imaging. These devices are designed to enhance patient positioning and stabilization during medical treatments.
Where is Reison Medical AB based?
Reison Medical AB is based in the United States. The company operates within U.S. regulatory frameworks, ensuring its devices comply with applicable requirements for medical device authorization in the country.
Which regulatory registries list Reison Medical AB’s devices?
Reison Medical AB’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices authorized for use in the U.S., including those manufactured by the company.
How are Reison Medical AB’s devices classified under U.S. regulations?
All devices produced by Reison Medical AB fall under Class I regulatory classification in the U.S. This classification applies to devices posing minimal risk to patients, such as reusable positioning and support devices, which are generally considered low-risk and subject to fewer regulatory controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 356766220
Catalogue (261)
Page 6 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cushion | 10-182 | FDA UDI | Class I | Active |
| Arm and leg guard | 10-554 | FDA UDI | Class I | Active |
| Widening section | 10-423 | FDA UDI | Class I | Active |
| Infusion stand rotating | 10-400-UK | FDA UDI | Class I | Active |
| Armboard short | 10-380-K-US | FDA UDI | Class I | Active |
| Arm/hand surgery table | 10-390-US | FDA UDI | Class I | Active |
| Patient barrier | 10-531-US | FDA UDI | Class I | Active |
| Instrument plate | 10-065 | FDA UDI | Class I | Active |
| Armboard | 10-380-M-10 | FDA UDI | Class I | Active |
| Widening section | 10-425-S | FDA UDI | Class I | Active |
| Safety side rail | 10-531 | FDA UDI | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Reison Medical Ab HALLSTAHAMMAR Vastmanland · SE FEI 3004414785