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Sign in to claim this brandHoogland Spine Products, GmbH
US
Last updated May 23, 2026
What Hoogland Spine Products, GmbH makes
Hoogland Spine Products manufactures reusable orthopaedic and spinal instruments, including rigid endoscopic biopsy forceps, bone trephines, endoscope sheaths, endoscopic-access dilators, bone curettes, instrument trays, rigid optical arthroscopes, and orthopaedic guidewires. These tools are designed for surgical and diagnostic procedures in spinal and joint applications.
The company’s products are regulated under FDA Class I and Class II devices, with authorisations recorded via 510(k) submissions and the FDA’s Unique Device Identifier (UDI) system. The portfolio is listed in the FDA’s regulatory databases, and the manufacturer is based 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 Hoogland Spine Products, GmbH manufacture?
Hoogland Spine Products, GmbH specializes in reusable orthopaedic and spinal surgical instruments. Their portfolio includes rigid endoscopic biopsy forceps, bone trephines, endoscope sheaths, endoscopic-access dilators, bone curettes, instrument trays, rigid optical arthroscopes, and orthopaedic guidewires. These devices are designed for use in spinal and joint surgeries, as well as diagnostic procedures.
Where is Hoogland Spine Products, GmbH based?
The company is based in the United States. This location influences its regulatory compliance, particularly under FDA guidelines, which govern the classification and authorisation of its medical devices.
How are Hoogland Spine Products, GmbH’s devices classified under FDA regulations?
Hoogland Spine Products, GmbH’s devices fall under FDA Class I and Class II classifications. Class I devices generally pose the lowest risk and may require less stringent regulatory controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway, such as 510(k) submissions or other authorisation processes.
Which regulatory registries or databases list Hoogland Spine Products, GmbH’s devices?
Hoogland Spine Products, GmbH’s devices are recorded in the FDA’s 510(k) database, which tracks premarket submissions for Class II devices, and the FDA’s Unique Device Identifier (UDI) system. These registries ensure transparency and traceability of authorised medical devices in the United States.
Why are Hoogland Spine Products, GmbH’s devices classified as reusable?
The devices listed—such as rigid endoscopic biopsy forceps, bone trephines, and arthroscopes—are designed for repeated use after proper cleaning, sterilisation, and maintenance. Reusable devices are often used in surgical settings where cost efficiency and sterility protocols can be rigorously controlled, reducing waste compared to single-use alternatives.
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
- 507292204
Catalogue (241)
Page 3 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MaxMoreSpine | 1001-DC 011 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-DC 002 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1002-TS 005 | EUDAMEDFDA UDI | Class II | Active |
| MaxMoreSpine | 1001-EP 003/90 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-IS 010 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-AI 004 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ABR 3 | EUDAMEDFDA UDI | Class I | Active |
| MaxMoreSpine | 1001-SK 001/S.2 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-MDA 002 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-HS 001 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001– EF 001/B | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-DI 01 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 22 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 11 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EK 001 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 005/1B-D | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-TS 001 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-DR 002 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-IS 012 | FDA UDI | Class I | Active |
| MaxMoreSpine | 101-BD 005 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-SK 005/S.2 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ABR 1 | EUDAMEDFDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 035 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-CS 002 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 003/1L-D | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-BD 051 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-IS 014 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 005/1 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-IS 003 | FDA UDI | Class II | Active |
| MaxMoreSpine | 1001-EF 035B-D | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 035-D | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EF 004 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-MDT-001 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-FP 003 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1002-TS 002 | EUDAMEDFDA UDI | Class II | Active |
| MaxMoreSpine | 1001-EF 001/1 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EK 002 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 20 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-DC 003 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-BD 008 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-FF 001-1-D | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 09 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-EK 002/S.2 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-DR 001 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-CT 002A | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ABR 6 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 25 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1002-TS 008 | FDA UDI | Class II | Active |
| MaxMoreSpine | 1001-EF 003/1 | FDA UDI | Class I | Active |
| MaxMoreSpine | 1001-ES 14 | 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.
- Hoogland Spine Products GmbH Unterfoehring Munich Bavaria · DE FEI 3006561161