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Sign in to claim this brandMORGAN STEER ORTHOPAEDICS LIMITED
US
Last updated May 30, 2026
Part of Morgan Steer Orthopaedics Ltd
What MORGAN STEER ORTHOPAEDICS LIMITED makes
The company manufactures single-use endoscopic electrosurgical electrodes, specifically bipolar models designed for minimally invasive spinal procedures, as well as single-use needle guides and cannulas for spinal interventions. Their portfolio includes devices like the SpineWand, a bipolar electrode for electrosurgical applications, and the Spine Needle and Cannula, used for precise needle placement in spinal surgeries.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.
Written from this company's registered devices by an AI model, 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
- 216776681
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SpineWand | SDC01-01 | FDA UDI | Class II | Active |
| SpineWand | K7920-01 | FDA UDI | Class II | Active |
| SpineWand | SDLR03-01 | FDA UDI | Class II | Active |
| Spine Needle and Cannula | SCL600-01 | FDA UDI | Class II | Active |
| Spine Needle and Cannula | SCL800-01 | FDA UDI | Class II | Active |
| SpineWand | SDLG03-01 | FDA UDI | Class II | Active |
| Spine Needle and Cannula | KNS-1904-10 | FDA UDI | Class II | Active |
| Spine Needle and Cannula | KNS-1706-10 | FDA UDI | Class II | Active |
| SpineWand | K7925-01 | FDA UDI | Class II | Active |
| SpineWand | SDC03-01 | FDA UDI | Class II | Active |
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