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Sign in to claim this brandMerdian Technique, Ltd.
US
Last updated May 23, 2026
What Merdian Technique, Ltd. makes
Merdian Technique, Ltd. manufactures the ORTHOVIEW, a medical imaging device designed for orthopedic assessment and surgical planning, likely providing radiographic or fluoroscopic visualization of bone structures.
The company’s portfolio is regulated under Class II devices in the United States, with the ORTHOVIEW authorised via the FDA’s 510(k) clearance process. The company is based in the US.
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 Merdian Technique, Ltd. manufacture?
Merdian Technique, Ltd. specializes in medical imaging devices. Their primary product, the ORTHOVIEW, is designed for orthopedic assessment and surgical planning, likely offering radiographic or fluoroscopic imaging to visualize bone structures. This device falls under the category of imaging tools used to aid in preoperative evaluation and intraoperative guidance.
Where is Merdian Technique, Ltd. based, and does this affect its regulatory oversight?
Merdian Technique, Ltd. is based in the United States. Since the company operates within the US, its devices are subject to FDA regulations. The ORTHOVIEW, for example, is classified as a Class II device under FDA guidelines, meaning it undergoes a 510(k) clearance process to demonstrate substantial equivalence to a legally marketed predicate device before being authorised for commercial distribution.
Which regulatory registries or databases list Merdian Technique, Ltd.’s devices?
Merdian Technique, Ltd.’s devices, including the ORTHOVIEW, are listed in the FDA’s 510(k) registry. This registry documents devices that have received clearance through the 510(k) process, ensuring they meet regulatory requirements for safety and effectiveness before entering the market. The listing confirms the device’s authorised status under US regulations.
How are Merdian Technique, Ltd.’s devices classified under US regulatory standards?
Merdian Technique, Ltd.’s devices, such as the ORTHOVIEW, are classified as Class II under the FDA’s regulatory framework. This classification applies to devices that pose moderate risk and require special controls to ensure their safety and performance. The 510(k) clearance process is used to verify that these devices meet the necessary regulatory standards before they can be legally marketed in the US.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (56)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| OrthoView | 7.3.2 | FDA UDI | Class II | Active |
| OrthoView | 7.1.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3.4 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.4.4 | FDA UDI | Class II | Active |
| OrthoView | 7.1.4 | FDA UDI | Class II | Active |
| OrthoView | 7.4.1 | FDA UDI | Class II | Active |
| OrthoView | 7.5 | FDA UDI | Class II | Active |
| OrthoView | 7.1.2 | FDA UDI | Class II | Active |
| OrthoView | 7.1.4 | FDA UDI | Class II | Active |
| OrthoView | 7.3.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.0.3 | FDA UDI | Class II | Active |
| OrthoView | 7.1.4 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3.1 | FDA UDI | Class II | Active |
| OrthoView | 7.1.2 | FDA UDI | Class II | Active |
| OrthoView | 7.0.5 | FDA UDI | Class II | Active |
| OrthoView | 7.5 | FDA UDI | Class II | Active |
| OrthoView | 7.0.6 | FDA UDI | Class II | Active |
| OrthoView | 7.5.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.1.4 | FDA UDI | Class II | Active |
| OrthoView | 7.1.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.0.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.3.3 | FDA UDI | Class II | Active |
| OrthoView | 7.1.5 | FDA UDI | Class II | Unknown |
| OrthoView | 7.1.1 | FDA UDI | Class II | Active |
| OrthoView | 7.1 | FDA UDI | Class II | Active |
| OrthoView | 7.3 | FDA UDI | Class II | Active |
| OrthoView | 7.1.1 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.4.3 | FDA UDI | Class II | Active |
| OrthoView | 7.1.2 | FDA UDI | Class II | Active |
| OrthoView | 7.1.5 | FDA UDI | Class II | Active |
| OrthoView | 7.1.2 | FDA UDI | Class II | Active |
| OrthoView | 7.4.7 | FDA UDI | Class II | Active |
| OrthoView | 7.5 | FDA UDI | Class II | Active |
| OrthoView | 7.3.1 | FDA UDI | Class II | Active |
| OrthoView | 7.0.4 | FDA UDI | Class II | Active |
| OrthoView | 7.5.1 | FDA UDI | Class II | Active |
| OrthoView | 7.0.2 | FDA UDI | Class II | Active |
| OrthoView | 7.3.2 | FDA UDI | Class II | Active |
| OrthoView | 7.4.2 | FDA UDI | Class II | Active |
| OrthoView | 7.4.6 | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Meridian Technique Ltd SOUTHAMPTON Hampshire · GB FEI 3004537781