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LiteCure Lightforce Deep Tissue Laser Therapyโ„ข System - HSA Registration DE0501920

Access comprehensive regulatory information for LiteCure Lightforce Deep Tissue Laser Therapyโ„ข System in the Singapore medical device market through Pure Global AI's free database. This CLASS C medical device is registered under HSA registration number DE0501920 and owned by LiteCure LLC. The device was registered on July 19, 2018.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS C
DE0501920
LiteCure Lightforce Deep Tissue Laser Therapyโ„ข System
HSA Registration Number: DE0501920
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Product Description

To provide topical heating for the purpose of elevating tissue temperature for a temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; the temporary relaxation of muscle.

Device Classification
Device Class
CLASS C
Medical Speciality Area
General & Plastic Surgery
Registration Information
Registration Number
DE0501920
Registration Date
July 19, 2018
Change Notification Approval Date
October 11, 2019
Retention Due Date
July 18, 2025
Product Owner
Short Name
LiteCure LLC
Address
101 Lukens Dr, Suite A, New Castle, DE 19720, UNITED STATES
Registrant
Address
22 SIN MING LANE, MIDVIEW CITY, #07-88, SINGAPORE 573969
Importer
Address
22 SIN MING LANE, MIDVIEW CITY, #07-88, SINGAPORE 573969
Model Information
Model Name(s)
Lightforce FXi Lightforce PRO
Model Identifier(s)
LTC-1500 LTC-900