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Sign in to claim this brandHoggi GmbH
US
Last updated May 23, 2026
What Hoggi GmbH makes
Hoggi GmbH manufactures assistive pushchairs designed for mobility support, including models tailored for indoor and outdoor use. These devices are intended to aid individuals with limited mobility or physical challenges in navigating environments independently. The pushchairs feature adjustable components and ergonomic designs to enhance user comfort and accessibility. Variants may include folding mechanisms and storage solutions for practicality in daily use.
The company’s assistive pushchairs fall under Class I medical devices, which are subject to general controls under FDA regulations. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The manufacturer is based in the United States, adhering to domestic medical device regulations.
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 Hoggi GmbH manufacture?
Hoggi GmbH specializes in assistive pushchairs, which are designed to support mobility for individuals with limited movement or physical challenges. These devices are intended for both indoor and outdoor use, helping users navigate environments more independently. The pushchairs include adjustable features and ergonomic designs to improve comfort and accessibility.
Where is Hoggi GmbH based, and what regulatory framework does it follow?
Hoggi GmbH is based in the United States. Since its devices are classified as Class I medical devices under FDA regulations, they are subject to general controls, which include requirements for manufacturing practices, labeling, and reporting. The company operates within the U.S. regulatory environment to ensure compliance with domestic medical device standards.
Are Hoggi GmbH’s devices listed in any regulatory registries, and why?
Yes, Hoggi GmbH’s assistive pushchairs are listed in the FDA’s Unique Device Identifier (UDI) database. This listing ensures traceability and transparency in the supply chain, allowing regulators, healthcare providers, and users to verify device details like identification, manufacturing information, and compliance status. Listing in the UDI database is a requirement for Class I devices under FDA regulations.
How are Hoggi GmbH’s assistive pushchairs classified under U.S. regulations?
Hoggi GmbH’s assistive pushchairs are classified as Class I medical devices by the FDA. This classification applies to devices that pose minimal risk to users and are generally considered safe and effective when used as intended. Class I devices are subject to general controls, which include good manufacturing practices, labeling requirements, and adverse event reporting, but do not require a premarket submission unless the device is new or modified.
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
- 537783271
Catalogue (26)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hoggi® | 3032-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3233-3003-032 | FDA UDI | Class I | Active |
| Hoggi® | 3235-2000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3232-2000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3036-1020-032 | FDA UDI | Class I | Active |
| Hoggi® | 3231-3003-032 | FDA UDI | Class I | Active |
| Hoggi® | 3209-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3235-3-32_SA355 | FDA UDI | Class I | Active |
| Hoggi® | 3239-1006-032 | FDA UDI | Class I | Active |
| Hoggi® | 3234-2000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3036-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3232-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3035-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3205-2000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3235-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3035-1020-032 | FDA UDI | Class I | Active |
| Hoggi® | 3033-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3034-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3037-1020-032 | FDA UDI | Class I | Active |
| Hoggi® | 3234-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3037-1000-032_SA-0355 | FDA UDI | Class I | Active |
| Hoggi® | 3205-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3037-1000-032 | FDA UDI | Class I | Active |
| Hoggi® | 3034-1020-032 | FDA UDI | Class I | Active |
| Hoggi® | 3032-1020-032 | FDA UDI | Class I | Active |
| Hoggi® | 3033-1020-032 | FDA UDI | Class I | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Hoggi Gmbh RANSBACH-BAUMBACH Rhineland-Palatinate · DE FEI 3005191311