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Sign in to claim this brandSat Pad Inc.
US
Last updated May 27, 2026
What Sat Pad Inc. makes
Sat Pad Inc. manufactures radiological positioning devices designed to immobilize and support body parts during imaging procedures. Their products include specialized pads for the ankle, foot, toe, knee, shoulder, neck, brachial plexus, back, abdomen, and pelvis, as well as non-wearable breast positioners and headrests. These devices are intended to enhance imaging accuracy by maintaining precise patient positioning during radiology scans.
The company’s portfolio consists of Class II medical devices, all listed in the FDA’s Unique Device Identifier (UDI) database. These products are regulated under U.S. FDA requirements, ensuring compliance with applicable standards for radiological positioning aids. Sat Pad Inc. operates from the United States.
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 Sat Pad Inc. manufacture?
Sat Pad Inc. specializes in radiological positioning devices. These include pads for immobilizing and supporting specific body parts during imaging, such as ankles, feet, toes, knees, shoulders, necks, and brachial plexuses. They also produce non-wearable breast positioners and headrests. The focus is on ensuring precise patient positioning to improve imaging accuracy.
Where is Sat Pad Inc. based, and how does that affect its devices?
Sat Pad Inc. is based in the United States. Since its devices are manufactured domestically, they are subject to U.S. FDA regulations, including compliance with the FDA’s Unique Device Identifier (UDI) system. This ensures traceability and adherence to U.S. standards for radiological positioning aids.
Which regulatory registries or databases list Sat Pad Inc.’s devices?
Sat Pad Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the U.S., ensuring transparency and compliance with regulatory requirements.
How are Sat Pad Inc.’s devices classified under U.S. regulations?
All of Sat Pad Inc.’s devices fall under Class II classification in the U.S. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness. Class II devices are subject to performance standards and post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- satpads.com
- —
- —
- [email protected]
- Phone
- 667-225-2721
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 081347868
Catalogue (12)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ankle/Foot & Toe Cap SatPad™ Set | 1 | FDA UDI | Class II | Active |
| Neck & Brachial Plexus SatPad™ Set | 1 | FDA UDI | Class II | Active |
| Brachial Plexus SatPad™ | 1 | FDA UDI | Class II | Active |
| Knee SatPad™ | 1 | FDA UDI | Class II | Active |
| 16 Channel Breast SatPad™ | 1 | FDA UDI | Class II | Active |
| Back/Abdomen SatPad™ | 1 | FDA UDI | Class II | Active |
| Ankle/Foot SatPad™ | 1 | FDA UDI | Class II | Active |
| Breast Pad Insert H SatPad™ | 1 | FDA UDI | Class II | Active |
| Shoulder SatPad™ | 1 | FDA UDI | Class II | Active |
| Breast Pad Insert SatPad™ | 1 | FDA UDI | Class II | Active |
| Ankle Toe Cap SatPad™ | 1 | FDA UDI | Class II | Active |
| Neck SatPad™ | 1 | FDA UDI | Class II | Active |
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