Singapore HSA registration DE0501920
LiteCure Lightforce Deep Tissue Laser Therapy™ System
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 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.
Product Owner
- Name
- LiteCure LLC
- 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
About this record
Access comprehensive regulatory information for LiteCure Lightforce Deep Tissue Laser Therapy™ 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.
Free DatabasePowered by Pure Global AIHSA Official DataCLASS C