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Sign in to claim this brandSilony Medical GmbH
US
Last updated May 23, 2026
What Silony Medical GmbH makes
Silony Medical GmbH manufactures spinal fixation devices, including non-bioabsorbable bone screws, metallic and polymeric spinal interbody fusion cages, and components for internal spinal fixation systems such as rods and connectors. These products are designed for surgical use in spinal stabilization and fusion procedures, with some items supplied in sterile packaging.
The company’s devices fall under FDA Class II classification and are listed in the FDA’s Unique Device Identification (UDI) system. 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 Silony Medical GmbH manufacture?
Silony Medical GmbH specializes in spinal fixation devices. These include non-bioabsorbable bone screws, metallic and polymeric spinal interbody fusion cages, as well as components like rods, connectors, and other hardware for internal spinal fixation systems. The devices are primarily intended for surgical use in spinal stabilization and fusion procedures, with some items packaged sterilely for direct patient use.
Where is Silony Medical GmbH based?
Silony Medical GmbH is headquartered in the United States. The company’s location is relevant for regulatory oversight and compliance, as it operates under the jurisdiction of U.S. medical device regulations.
Which regulatory registries list Silony Medical GmbH’s devices?
Silony Medical GmbH’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and track specific devices by their unique identifiers.
How are Silony Medical GmbH’s devices classified by regulatory authorities?
Silony Medical GmbH’s devices are classified as FDA Class II. This classification is determined based on the level of risk associated with the device. Class II devices generally require special controls in addition to general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
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
- 342538826
Catalogue (1729)
Page 3 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Verticale | S-VML-6245-RF2 | FDA UDI | Class II | Active |
| Roccia | S-RTT-13341215-S | FDA UDI | Class II | Active |
| Verticale | S-VPS-5260-S2 | FDA UDI | Class II | Active |
| Verticale | S-VFS-5245-KF1 | FDA UDI | Class II | Active |
| Roccia | S-RCP-06181351-S | FDA UDI | Class II | Active |
| Verticale | S-VIS-8210-RF2 | FDA UDI | Class II | Active |
| Roccia | S-RAT-17342515-S | FDA UDI | Class II | Active |
| Verticale | S-VCF-4054-K | FDA UDI | Class II | Active |
| Verticale | S-VML-7250-S2 | FDA UDI | Class II | Active |
| Verticale | S-VCF-4040-K | FDA UDI | Class II | Active |
| Verticale | S-VMS-7020 | FDA UDI | Class II | Active |
| Roccia | S-RUT-155810-S | FDA UDI | Class II | Active |
| Favo | S-FST-15113805-S | FDA UDI | Class II | Active |
| Verticale | S-VPS-7270-S2 | FDA UDI | Class II | Active |
| Verticale | S-VIS-0290-S1 | FDA UDI | Class II | Active |
| Verticale | S-VUS-5225-RS2 | FDA UDI | Class II | Active |
| Verticale | S-VML-5250-RS2 | FDA UDI | Class II | Active |
| Roccia | S-RCP-06181305-S | FDA UDI | Class II | Active |
| Roccia | S-RAT-15403115-S | FDA UDI | Class II | Active |
| Verticale | S-VML-7260-S2 | FDA UDI | Class II | Active |
| Favo | S-FST-12113305-S | FDA UDI | Class II | Active |
| Roccia | S-RTT-15401310-S | FDA UDI | Class II | Active |
| Verticale | S-VUS-6250-S1 | FDA UDI | Class II | Active |
| Verticale | S-VML-4535-K2 | FDA UDI | Class II | Active |
| Verticale | S-VUS-6230-S1 | FDA UDI | Class II | Active |
| Verticale | S-VFS-0280-RS2 | FDA UDI | Class II | Active |
| Verticale | S-VPS-8275-RS3 | FDA UDI | Class II | Active |
| Verticale | S-VIS-8250-KF1 | FDA UDI | Class II | Active |
| Roccia | S-RAT-15342520-S | FDA UDI | Class II | Active |
| Roccia | S-RCP-07181305-S | FDA UDI | Class II | Active |
| Favo | S-FST-14113315-S | FDA UDI | Class II | Active |
| Verticale | S-VIS-0260-RF2 | FDA UDI | Class II | Active |
| Verticale | S-VOS-4514-3 | FDA UDI | Class II | Active |
| Verticale | S-VPS-9230-RS3 | FDA UDI | Class II | Active |
| Verticale | S-VFS-4545-K1 | FDA UDI | Class II | Active |
| Verticale | S-VFS-5225-RK2 | FDA UDI | Class II | Active |
| Verticale | S-VPS-7245-S2 | FDA UDI | Class II | Active |
| Verticale | S-VPS-6225-K2 | FDA UDI | Class II | Active |
| Verticale | S-VFS-8250-RS2 | FDA UDI | Class II | Active |
| Verticale | S-VFS-5225-K1 | FDA UDI | Class II | Active |
| Verticale | S-VFS-8230-RK2 | FDA UDI | Class II | Active |
| Favo | S-FST-10112800-S | FDA UDI | Class II | Active |
| Verticale | S-VCF-4024-SG | FDA UDI | Class II | Active |
| Roccia | S-RTT-09281110-S | FDA UDI | Class II | Active |
| Verticale | S-VFS-0240-RF2 | FDA UDI | Class II | Active |
| Verticale | S-VPS-9245-KF2 | FDA UDI | Class II | Active |
| Verticale | S-VFS-0280-S1 | FDA UDI | Class II | Active |
| Roccia | S-RUT-104005-S | FDA UDI | Class II | Active |
| Verticale | S-VFS-5235-KF1 | FDA UDI | Class II | Active |
| Verticale | S-VFS-0210-RS2 | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Silony Medical Gmbh Leinfelden-Echterdingen Baden-Wurttemberg · DE FEI 3013422236