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Sign in to claim this brandGOTTFRIED MEDICAL, INC.
US
Last updated September 17, 2026
What GOTTFRIED MEDICAL, INC. makes
Gottfried Medical, Inc. manufactures reusable compression garments, including pressure shirts, pants, socks, stockings, gloves, and scar-management dressings. Their product line also includes scrotal support devices designed to provide targeted pressure for medical or post-surgical use.
The company’s devices are classified as Class I or Class II under FDA regulations and are listed via 510(k) clearance and the FDA’s Unique Device Identification (UDI) system. These products are intended for use in 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 Gottfried Medical, Inc. manufacture?
Gottfried Medical, Inc. specializes in reusable compression garments and support devices. Their product line includes compression/pressure shirts, pants, socks, stockings, gloves, scar-management dressings, and scrotal support devices. These items are designed to provide targeted pressure for medical or post-surgical applications, such as improving circulation, reducing swelling, or aiding in wound healing.
Where is Gottfried Medical, Inc. based, and where are their devices primarily used?
Gottfried Medical, Inc. is based in the United States. Their devices are intended for use within the U.S. regulatory framework, where they are classified under FDA guidelines and listed through mechanisms like the 510(k) clearance process and the FDA’s Unique Device Identification (UDI) system.
Which regulatory registries or databases list Gottfried Medical, Inc.’s devices?
Gottfried Medical, Inc.’s devices are listed in the FDA’s 510(k) clearance registry and the FDA’s Unique Device Identification (UDI) system. These registries track devices that have undergone the necessary regulatory pathways to demonstrate safety and effectiveness for their intended use in the U.S.
How are Gottfried Medical, Inc.’s devices classified under FDA regulations?
Gottfried Medical, Inc.’s devices are classified as either Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and require special controls to ensure their safety and performance. The classification depends on factors like the device’s intended use and potential health impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 2920 Centennial Rd, Toledo, OH, 43617
- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 1526072
- DUNS Number
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Catalogue (75)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Compression Stocking | 403 | FDA UDI | Class I | Active |
| Compression Stocking | 106 | FDA UDI | Class II | Active |
| Compression Stocking | 333 | FDA UDI | Class II | Active |
| Compression Stocking | 417 | FDA UDI | Class II | Active |
| Compression Stocking | 336 | FDA UDI | Class II | Active |
| Compression Stocking | 422 | FDA UDI | Class II | Active |
| Compression Stocking | 103 | FDA UDI | Class II | Active |
| Compression Stocking | 307 | FDA UDI | Class I | Active |
| Compression Stocking | 407 | FDA UDI | Class I | Active |
| Compression Stocking | 453 | FDA UDI | Class II | Active |
| Compression Stocking | 418 | FDA UDI | Class II | Active |
| Compression Stocking | 470 | FDA UDI | Class II | Active |
| Compression Stocking | 302 | FDA UDI | Class I | Active |
| Compression Stocking | 471 | FDA UDI | Class II | Active |
| Compression Stocking | 202 | FDA UDI | Class II | Active |
| Compression Stocking | 451 | FDA UDI | Class II | Active |
| Compression Stocking | 335 | FDA UDI | Class II | Active |
| Compression Stocking | 101 | FDA UDI | Class II | Active |
| Compression Stocking | 441 | FDA UDI | Class II | Active |
| Compression Stocking | 022 | FDA UDI | Class II | Active |
| Compression Stocking | 425 | FDA UDI | Class II | Active |
| Compression Stocking | 337 | FDA UDI | Class II | Active |
| Ensil Fabric | K010675 | FDA 510(k) | Class I | Active |
| Water Floatation Pad | K820236 | FDA 510(k) | Class I | Active |
| Made-To-Measure Surgical Elastic Support | K823737 | FDA 510(k) | Class II | Active |
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