LZ30 LZ30-ProR

• FDA 510(k) K123474 decided 3 Dec 2013 Active
• FDA GUDID UDI-DI 00852116008032 listed 3 Mar 2022 Listed

1. 3 Dec 2013 Cleared FDA 510(k) K123474
2. 3 Mar 2022 Listed FDA GUDID 00852116008032

Trade name

LZ30

Generic name

Musculoskeletal/physical therapy laser, professional

Model / reference

LZ30-ProR

Primary DI / UDI-DI

00852116008032

510(k) Number

K123474 ↗

FDA product code

ILY

GMDN term

Musculoskeletal/physical therapy laser, professional

Device class

Class II

Regulation number

890.5500

GUDID distribution status

Not in Commercial Distribution

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

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• ANTI-WRINKLE LIGHT, MODEL 1302 AND PAIN THERAPY LIGHT, MODEL 1301 by LED Intellectual Properties
• L-SER KO LAMP by Ya-Man, Ltd.
• MAESTRO MDTL LASER SYSTEM by Advanced Medical Technologies AG
• WS FAR INFRARED THERAPY UNIT, MODEL # TY-101 SERIES by Ws Far IR Medical Technology Co., Ltd.
• LIGHT PATCH by Bioscan, Inc.
• WS(TM) Far-Infrared Therapy Unit, Model KP-B210 by Ws Far IR Medical Technology Co., Ltd.
• MODEL 2200 by Clarimedex, Inc.
• TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS by Escada International, Inc.
• ASA 'MPHI FAMILY DIODE LASER by Cynosure, LLC

• LZ30 LZ30 MaxR

  Class II

  FDA 510(k) K123474 Active Cleared 3 Dec 2013 GUDID on market

• LZ30 LZ30 MaxIR

  Class II

  FDA 510(k) K123474 Active Cleared 3 Dec 2013 GUDID on market

• LZ30 LZ30 GrIR

  Class II

  FDA 510(k) K123474 Active Cleared 3 Dec 2013 GUDID on market

• LZ30 LZ30 ProZ-Vet

  Class II

  FDA 510(k) K123474 Active Cleared 3 Dec 2013 GUDID on market

See all devices from Avant Wellness Systems Inc →