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LightForce FX LTC-1500

by Litecure LLC

LightForce FX LTC-1500 is a Class II device made by Litecure LLC, listed in FDA GUDID since 7 Feb 2017 (UDI-DI 00854103007011), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854103007011 UDI-DI Date7 Feb 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
LightForce FX
Generic name
Musculoskeletal infrared phototherapy unit, non-wearable
Model / reference
LTC-1500
Primary DI / UDI-DI
00854103007011
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

Related devices

Category: Musculoskeletal infrared phototherapy unit, non-wearable

Similar devices

Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).

Other devices from Litecure LLC

See all devices from Litecure LLC →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)