LightForce PRO LTC-900
by Litecure LLC
LightForce PRO LTC-900 is a Class II device made by Litecure LLC, listed in FDA GUDID since 7 Feb 2017 (UDI-DI 00854103007004), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00854103007004 | Date7 Feb 2017 | StatusListed |
Official records
- AccessGUDID record 00854103007004
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LightForce PRO
- Generic name
- Musculoskeletal infrared phototherapy unit, non-wearable
- Model / reference
- LTC-900
- Primary DI / UDI-DI
- 00854103007004
- FDA product code
- ILY
- GMDN term
- Musculoskeletal infrared phototherapy unit, non-wearable
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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