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US
Last updated May 24, 2026
What Söring GmbH makes
Söring GmbH manufactures reusable handpieces and generators for soft-tissue ultrasonic surgical systems. These devices include handpieces like the MS-Pen and UAW Instrument, designed for precision cutting and coagulation in surgical procedures, alongside ultrasonic generators such as the SONOCA 300 and SONOCA 185.
The company’s portfolio is regulated under FDA’s Class II and Unclassified (U) device classifications, with products listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer 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 Söring GmbH manufacture?
Söring GmbH specializes in reusable ultrasonic surgical systems for soft-tissue procedures. Their portfolio includes handpieces like the MS-Pen and UAW Instrument, which are used for precise cutting and coagulation, as well as ultrasonic generators such as the SONOCA 300 and SONOCA 185. These devices are designed to assist surgeons in minimally invasive and controlled tissue manipulation.
Where is Söring GmbH based?
Söring GmbH operates from the United States. While the company’s headquarters or primary location isn’t specified, its regulatory filings and device listings confirm its presence and operations within the country.
Which regulatory registries or databases list Söring GmbH’s devices?
Söring GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, ensuring they can verify the identity and specifications of the company’s ultrasonic surgical systems.
How are Söring GmbH’s devices classified under FDA regulations?
Söring GmbH’s devices fall under FDA’s Class II and Unclassified (U) classifications. Class II devices generally pose moderate risk and require special controls to ensure safety and effectiveness, while Unclassified devices may require additional scrutiny based on their specific use or potential risks. These classifications guide regulatory oversight and compliance requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- soering.com
- —
- —
- [email protected]
- Phone
- 844 476 7464
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 322238346
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| MS-Pen | 92-021 | FDA UDI | Class II | Active |
| Pen | 91-020 | FDA UDI | Class II | Unknown |
| MS-Pen | 92-020 | FDA UDI | Class II | Active |
| UAW Instrument | 97-102 | FDA UDI | U | Active |
| Lud | 94-054 | FDA UDI | Class II | Unknown |
| MS-Pen | 92-112 | FDA UDI | Class II | Active |
| Arco-Multifunctional-Instrument | 53-027 | FDA UDI | Class II | Unknown |
| Mbc 200 | M200-0000B-FL | FDA UDI | Class II | Unknown |
| Bcc 140 | B140-0000B-FL | FDA UDI | Class II | Unknown |
| Enp | 92-030 | FDA UDI | Class II | Unknown |
| Arco 3000 | 68-000B-FL | FDA UDI | Class II | Unknown |
| Pen | 91-021 | FDA UDI | Class II | Unknown |
| Sonoca 300 | 15-000B-FL | FDA UDI | Class II | Active |
| UAW Instrument | 97-104 | FDA UDI | U | Active |
| Sonoca 185 | S185-000B-FL | FDA UDI | U | Active |
| UAW Instrument | 97-112 | FDA UDI | U | Active |
| Mbc 601 Uam | 88-000B-UAM-FL | FDA UDI | Class II | Unknown |
| UAW Instrument | 97-103 | FDA UDI | U | Active |
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