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Sign in to claim this brandLccs Products Limited
US
Last updated May 27, 2026
What Lccs Products Limited makes
Lccs Products Limited manufactures spinal needles designed for single-use procedures, as well as non-threaded epidural needles for medical interventions. The company also produces percutaneous radio-frequency ablation probes, including monopolar denervation variants available in both reusable and single-use configurations, alongside reusable electrical connection cables for medical devices.
All listed devices fall under Class II regulatory classification in the US, with authorisations obtained through FDA 510(k) submissions and FDA’s Unique Device Identification (UDI) system. The company is based in the United States and its products are tracked within these regulatory frameworks.
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 Lccs Products Limited manufacture?
Lccs Products Limited specializes in devices primarily used in interventional and pain management procedures. Their portfolio includes single-use spinal needles for precise injections, non-threaded epidural needles for targeted medical interventions, and percutaneous radio-frequency ablation probes—both reusable and single-use—designed for monopolar denervation. Additionally, they produce reusable electrical-only medical device connection cables, which facilitate safe and reliable electrical connections in clinical settings.
Where is Lccs Products Limited based, and how does this affect its regulatory oversight?
Lccs Products Limited is based in the United States, which means its devices are subject to FDA regulatory requirements. Since all listed devices fall under Class II classification, they must comply with FDA’s 510(k) premarket notification process and the Unique Device Identification (UDI) system to ensure traceability and safety standards are met.
Which regulatory registries or databases list Lccs Products Limited’s devices?
Lccs Products Limited’s devices are tracked within the FDA 510(k) database and the FDA Unique Device Identification (UDI) system. These registries ensure transparency in device authorisation, classification, and compliance with U.S. medical device regulations, allowing healthcare providers and regulators to verify product details and approval status.
How are Lccs Products Limited’s devices classified under U.S. regulations, and why does this matter?
All of Lccs Products Limited’s devices are classified as Class II under FDA regulations. This classification indicates a moderate level of risk, requiring compliance with specific controls to ensure safety and effectiveness. Class II devices must undergo 510(k) premarket submissions to demonstrate substantial equivalence to legally marketed predicates, ensuring they meet established performance standards before entering the market.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- lccsmedical.com
- —
- —
- [email protected]
- Phone
- +1 (844) 743-6449
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 663190222
Catalogue (230)
Page 5 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lccs | S-1510-18-LC | FDA UDI | Class II | Active |
| Lccs | SS2790-LC | FDA UDI | Class II | Active |
| Lccs | C-505-22-LC | FDA UDI | Class II | Active |
| Lccs | SQ2790-LC | FDA UDI | Class II | Active |
| Lccs | IKD-D-30-LC | FDA UDI | Class II | Active |
| Lccs | SQ2250-LC | FDA UDI | Class II | Active |
| Lccs | SS2650-I-LC | FDA UDI | Class II | Active |
| Lccs | C-1010-Y-16-LC | FDA UDI | Class II | Active |
| Lccs | SS2250-LC | FDA UDI | Class II | Active |
| Lccs | SS2490-LC | FDA UDI | Class II | Active |
| Lccs | SQ23125-LC | FDA UDI | Class II | Active |
| Lccs | SS24155-I-LC | FDA UDI | Class II | Active |
| Lccs | C-1005-18-LC | FDA UDI | Class II | Active |
| Lccs | SS24125-LC | FDA UDI | Class II | Active |
| Lccs | RE27150-R-LC | FDA UDI | Class II | Active |
| Lccs | SS22120-LC | FDA UDI | Class II | Active |
| Lccs | IKD-S-30-LC | FDA UDI | Class II | Active |
| Lccs | ET1790-D-LC | FDA UDI | Class II | Active |
| Lccs | C-1010-S-22-LC | FDA UDI | Class II | Active |
| Lccs | S-1005-18-LC | FDA UDI | Class II | Active |
| Lccs | C-1010-B-20-LC | FDA UDI | Class II | Active |
| Lccs | RE27200-D-LC | FDA UDI | Class II | Active |
| Lccs | C-1010-S-16-LC | FDA UDI | Class II | Active |
| Lccs | C-505-B-20-LC | FDA UDI | Class II | Active |
| Lccs | RE2750-R-LC | FDA UDI | Class II | Active |
| Single Use Grounding Pad | K132136 | FDA 510(k) | Class II | Active |
| LCCS Disposable RF Electrode, LCCS Reusable RF Electrode | K152642 | FDA 510(k) | Class II | Active |
| LCCS VC-S RF Cannula | K191293 | FDA 510(k) | Class II | Active |
| Lccs Insulated Spinal Needle (rf Cannula) | K112231 | FDA 510(k) | Class II | Active |
| Anesthesia Conduction Needles | K131006 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Lccs Products Limited SAI YING PUN · HK FEI 3009241989