LightForce FXi LTC-1500
by Litecure LLC
LightForce FXi LTC-1500 is a Class II device made by Litecure LLC, listed in FDA GUDID since 24 Jul 2017 (UDI-DI 00854103007042), 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 | Number00854103007042 | Date24 Jul 2017 | StatusListed |
Official records
- AccessGUDID record 00854103007042
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- LightForce FXi
- Generic name
- Musculoskeletal/physical therapy laser, professional
- Model / reference
- LTC-1500
- Primary DI / UDI-DI
- 00854103007042
- FDA product code
- ILY
- GMDN term
- Musculoskeletal/physical therapy laser, professional
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).
- HeatLux Pro II by Home Skinovations, Ltd.
- OLIZ LTB-1000A by Ltbio Co., Ltd.
- SACRED CRANE TDP by Telstar Innovations, Inc.
- KENKOWAVE INFRARED PAIN TREATMENT SYSTEM by Kaylight Corporation
- THERMAPULSE by Palomar Medical Products, Inc.
- TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS by Escada International, Inc.
- BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS by Meditech International Inc
- ALMA LASER NIR MODULE by ALMA LASERS LTD.
- NEUTROLUMENPN SYSTEM, MODEL 1000 by NEUROLUMEN LLC
- 3B Laser 500, 3B Laser 200, LA-X P 500, LA-X P 200 by Livetec GmbH