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Sign in to claim this brandMidtown Investments, LLC
US
Last updated May 25, 2026
What Midtown Investments, LLC makes
Midtown Investments, LLC manufactures single-use alternating-pressure bed mattress overlays designed to reduce pressure points and promote patient comfort during prolonged bed rest.
The company’s products are classified as Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database.
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 Midtown Investments, LLC manufacture?
Midtown Investments, LLC specializes in single-use alternating-pressure bed mattress overlays. These devices are designed to help reduce pressure points and improve patient comfort for individuals who require prolonged bed rest, such as hospital patients or those recovering at home.
Where is Midtown Investments, LLC based?
Midtown Investments, LLC is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.
How are the devices manufactured by Midtown Investments, LLC classified by regulatory authorities?
The devices produced by Midtown Investments, LLC fall under Class II classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, beyond general controls.
Are the devices manufactured by Midtown Investments, LLC listed in any regulatory registries?
Yes, the devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices by assigning a unique code to each product, ensuring better traceability and compliance with regulatory requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- 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
- —
- DUNS Number
- 180579414
Catalogue (20)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Matrix | Matrix-ALALMS42 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS42x8 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS8X48 | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS39 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS8X84 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS8 | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS84 | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS8 | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS42 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS39 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS42X84 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS48x84 | FDA UDI | Class II | Active |
| Matrix | Matrix-R/LALBDMS | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS84 | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS48 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALUMS | FDA UDI | Class II | Active |
| Matrix | Matrix-LALMS | FDA UDI | Class II | Active |
| Matrix | Matrix-R/LALBDMS48 | FDA UDI | Class II | Active |
| Matrix | Matrix-ALALMS48 | FDA UDI | Class II | Active |
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