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Sign in to claim this brandVIRTUAL PORTS LTD
US
Last updated May 24, 2026
What VIRTUAL PORTS LTD makes
Virtual Ports Ltd manufactures endoscopic retractors and retractors with integrated appliers, designed for minimally invasive surgical procedures. Their products include retractors with varying lengths (30cm and 45cm) and specialized tools like the EndoGrab and EndoLift for tissue manipulation. The ENDOCLEAR SYSTEM and its variants are also part of their portfolio, likely intended for clearing or cleaning purposes within endoscopic surgery.
The company’s devices are classified under FDA regulations as Class I and Class II, with submissions listed under 510(k) and UDI requirements. These products are intended for use in the United States, where they are subject to FDA oversight. No additional regulatory bodies or international listings are referenced in the provided data.
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 Virtual Ports Ltd manufacture?
Virtual Ports Ltd specializes in endoscopic retractors and retractors with integrated appliers. Their devices are designed for minimally invasive surgical procedures, including retractors with lengths of 30cm and 45cm, as well as specialized tools like the EndoGrab and EndoLift for tissue manipulation. They also produce systems like the ENDOCLEAR SYSTEM, which appears to be intended for clearing or cleaning within endoscopic surgery.
Where is Virtual Ports Ltd based, and where are their devices primarily regulated?
Virtual Ports Ltd is based in the United States. Their devices fall under FDA oversight, as indicated by their classification and regulatory submissions. The company’s products are listed under the FDA’s 510(k) and UDI (Unique Device Identification) requirements, meaning they are designed for use within the US market.
Which regulatory registries or databases list Virtual Ports Ltd’s devices?
Virtual Ports Ltd’s devices are listed in the FDA’s 510(k) premarket notification registry and the UDI database. These registries track devices that have undergone FDA review for compliance with US regulations, ensuring transparency in their classification and market authorization.
How are Virtual Ports Ltd’s devices classified under FDA regulations?
Virtual Ports Ltd’s devices are classified under two categories: Class I and Class II. Class I devices generally pose the lowest risk and may require less regulatory scrutiny, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the level of FDA oversight and documentation required for each product.
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
- 514870547
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Applier 30cm | AP030A | FDA UDI | Class I | Active |
| EndoGrab | EG000A | FDA UDI | Class I | Active |
| EndoGrab | EG000A | FDA UDI | Class I | Unknown |
| EndoGrab-Short | EGS00A | FDA UDI | Class I | Active |
| EndoLift | EL000A | EUDAMEDFDA UDI | Class I | Active |
| Applier 45cm | AP045A | FDA UDI | Class I | Active |
| Endoclear System | K100346 | FDA 510(k) | Class II | Active |
| Virtual Ports Endoclear System | K080051 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Virtual Ports Ltd Hod Hasharon Central · IL FEI 3006169466