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Lccs 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
—
LinkedIn
—
Facebook
—
Phone
+1 (844) 743-6449
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
663190222

Catalogue (230)

Page 1 of 5
DeviceModel / ReferenceRegistriesClassStatus
Lccs SS26101-I-LC
FDA UDI
Class IIActive
Lccs SS2270-LC
FDA UDI
Class IIActive
Lccs SQ22125-LC
FDA UDI
Class IIActive
Lccs RE2750-D-LC
FDA UDI
Class IIActive
Lccs C-1015-Y-22-LC
FDA UDI
Class IIActive
Lccs C-1515-B-22-LC
FDA UDI
Class IIActive
Lccs C-1010-Y-22-LC
FDA UDI
Class IIActive
Lccs ETE1790-LC
FDA UDI
Class IIActive
Lccs S-1502-20-LC
FDA UDI
Class IIActive
Lccs RE25200-D-LC
FDA UDI
Class IIActive
Lccs S-1005-S-20-LC
FDA UDI
Class IIActive
Lccs C-1510-B-22-LC
FDA UDI
Class IIActive
Lccs C-1010-S-20-LC
FDA UDI
Class IIActive
Lccs RE25100-D-LC
FDA UDI
Class IIActive
Lccs C-502-22-LC
FDA UDI
Class IIActive
Lccs C-1515-Y-18-LC
FDA UDI
Class IIActive
Lccs C-510-Y-18-LC
FDA UDI
Class IIActive
Lccs S-1510-20-LC
FDA UDI
Class IIActive
Lccs ET18113-D-LC
FDA UDI
Class IIActive
Lccs SS24101-I-LC
FDA UDI
Class IIActive
Lccs SQ2490-LC
FDA UDI
Class IIActive
Lccs RE27100-R-LC
FDA UDI
Class IIActive
Lccs C-510-Y-20-LC
FDA UDI
Class IIActive
Lccs SS22120-I-LC
FDA UDI
Class IIActive
Lccs C-1005-R-22-LC
FDA UDI
Class IIActive
Lccs ET22125-LC
FDA UDI
Class IIActive
Lccs SQ1690-LC
FDA UDI
Class IIActive
Lccs S-2005-20-LC
FDA UDI
Class IIActive
Lccs ET18155-D-LC
FDA UDI
Class IIActive
Lccs SS24101-LC
FDA UDI
Class IIActive
Lccs RE25150-R-LC
FDA UDI
Class IIActive
Lccs S-510-20-LC
FDA UDI
Class IIActive
Lccs ET2290-D-LC
FDA UDI
Class IIActive
Lccs SQ2390-LC
FDA UDI
Class IIActive
Lccs C-1510-18-LC
FDA UDI
Class IIActive
Lccs C-1010-R-20-LC
FDA UDI
Class IIActive
Lccs C-1510-S-22-LC
FDA UDI
Class IIActive
Lccs C-1505-S-18-LC
FDA UDI
Class IIActive
Lccs ET2090-D-LC
FDA UDI
Class IIActive
Lccs ET20155-LC
FDA UDI
Class IIActive
Lccs SS27125-LC
FDA UDI
Class IIActive
Lccs S-1010-18-LC
FDA UDI
Class IIActive
Lccs C-1505-20-LC
FDA UDI
Class IIActive
Lccs S-1510-22-LC
FDA UDI
Class IIActive
Lccs C-1510-Y-16-LC
FDA UDI
Class IIActive
Lccs C-510-Y-22-LC
FDA UDI
Class IIActive
Lccs ET1690-LC
FDA UDI
Class IIActive
Lccs SQ20113-LC
FDA UDI
Class IIActive
Lccs IKD-C-30-LC
FDA UDI
Class IIActive
Lccs SS25155-LC
FDA UDI
Class IIActive

Related Companies

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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