Litecure Therapy System
by Litecure LLC
510(k) K103511
Litecure Therapy System is a Class II device made by Litecure LLC, cleared under FDA 510(k) K103511 on 25 Jan 2011, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK103511 | Date25 Jan 2011 | StatusActive |
Official records
- FDA 510(k) database K103511
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ILY
- FDA applicant
- Litecure, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5500
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).
- ACUMED LASER, MODEL 1000 by Laser Thera, LLC
- SPINAL PAD by Bioscan, Inc.
- NovoTHOR XL 3.0 by THOR PHOTOMEDICINE INC.
- WEBERNEEDLE BASIC LASER by Weber Medical GmbH
- Laserpen Practise and Expert, Handylaser Sprint, Handylaser Trion, Physiolaser Olympic, Polylaser by Reimers & Janssen GmbH
- WS FREQUENCY SPECTRUM EFFECT PHYSIATRICS APPARATUS by C A I INDUSTRIES CORP
- LUMANOSITY CELEBRITY, MODEL 204 by Lumanosity, Inc.
- INFRARED LAMP by Harrier, Inc.
- RICH-MAR AUTOPRISM INFRARED LAMP by Rich-Mar Corp.
- MU PHOTONICS PAIN THERAPIST by Nu Photonics, Inc.