LightForce EXPi LTS-2500
by Litecure LLC
LightForce EXPi LTS-2500 is a Class II device made by Litecure LLC, listed in FDA GUDID since 24 Jul 2017 (UDI-DI 00854103007059), 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 | Number00854103007059 | Date24 Jul 2017 | StatusListed |
Official records
- AccessGUDID record 00854103007059
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LightForce EXPi
- Generic name
- Musculoskeletal/physical therapy laser, professional
- Model / reference
- LTS-2500
- Primary DI / UDI-DI
- 00854103007059
- FDA product code
- PDZ, ILY
- GMDN term
- Musculoskeletal/physical therapy laser, professional
- Device class
- Class II
- Regulation number
- 878.4810, 890.5500
- GUDID distribution status
- In Commercial Distribution
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