Avant Laser
by Avant Wellness Systems, LLC
510(k) K123474
Avant Laser is a Class II device made by Avant Wellness Systems, LLC, cleared under FDA 510(k) K123474 on 3 Dec 2013, 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 | NumberK123474 | Date3 Dec 2013 | StatusActive |
Official records
- FDA 510(k) database K123474
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- ILY
- Device class
- Class II
- Regulation
- 21 CFR Part 890.5500
- Advisory committee
- Physical Medicine
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K123474
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| LZ30 LZ30 GrIR | LZ30 GrIR | 00852116008155 | — | On the market |
| LZ30 LZ30 GRIV | LZ30 GRIV | 00852116008162 | — | On the market |
| LZ30 LZ30 GrVi | LZ30 GrVi | 00852116008148 | — | On the market |
| LZ30 LZ30 MaxIR | LZ30 MaxIR | 00852116008209 | — | On the market |
| LZ30 LZ30 MaxR | LZ30 MaxR | 00852116008193 | — | On the market |
| LZ30 LZ30 ProZ | LZ30 ProZ | 00852116008179 | — | On the market |
| LZ30 LZ30 ProZ-Vet | LZ30 ProZ-Vet | 00852116008100 | — | On the market |
| LZ30 LZ30 ReBl | LZ30 ReBl | 00852116008131 | — | On the market |
| LZ30 LZ30 Revi | LZ30 Revi | 00852116008186 | — | On the market |
| LZ30 LZ30 Revi-Home | LZ30 Revi-Home | 00852116008117 | — | On the market |
| LZ30 LZ30 Revi-Vet | LZ30 Revi-Vet | 00852116008124 | — | On the market |
| LZ30 LZ30 Z-Home | LZ30 Z-Home | 00852116008094 | — | On the market |
| LZ30 LZ30-Home | LZ30-Home | 00852116008070 | — | No longer on the market |
| LZ30 LZ30-P | LZ30-P | 00852116008025 | — | No longer on the market |
| LZ30 LZ30-ProIR | LZ30-ProIR | 00852116008049 | — | No longer on the market |
| LZ30 LZ30-ProR | LZ30-ProR | 00852116008032 | — | No longer on the market |
| LZ30 LZ30-ProX | LZ30-ProX | 00852116008063 | — | No longer on the market |
| LZ30 LZ30-ProZ | LZ30-ProZ | 00852116008056 | — | No longer on the market |
| LZ30 LZ30-Revi | LZ30-Revi | 00852116008087 | — | No longer on the market |
| LZ30 LZ30-X | LZ30-X | 00852116008018 | — | No longer on the market |
| LZ30 LZ30-Z | LZ30-Z | 00852116008001 | — | No longer on the market |
Similar devices
Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).
- 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
- COLD LIGHT; COLD LIGHT MD; GOSSAMER DERMLIGHT by ONYX MEDICAL LLC
- INFRALUX HEAT LAMP by Infralux International, Inc.
- PAINACEA MODEL XR8 INFRARED HEAT LAMP by Atlantis Luminescent Products, LLC
- DYNATRON TRI-WAVE LIGHT PAD DYNATRON TRI-WAVE LIGHT PROBE by Dynatronics Corp.
- PHOTONIC STIMULATOR by Bales Scientific, Inc.