# Innotech USA, Inc.

- Location (FDA's records): Washington, Dc, DC
- FDA decisions: 3 (2000–2004): 3 510(k) clearances
- Product codes: GEX (3)
- Predicates its devices cite: 13 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Candela Corp.: 2 (https://510kreport.com/company/candela)
- Laserscope: 2 (https://510kreport.com/company/laserscope)
- Cell Robotics, Inc.: 2 (https://510kreport.com/company/cell-robotics)
- Altus Medical, Inc.: 1 (https://510kreport.com/company/altus-medical)
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)
- Continuum Biomedical, Inc.: 1 (https://510kreport.com/company/continuum-biomedical)
- Continuum Electro-Optics, Inc.: 1 (https://510kreport.com/company/continuum-electro-optics)
- Cooltouch Corp.: 1 (https://510kreport.com/company/cooltouch)

## Firms that cite its devices most
- Msq (M2), Ltd.: 2 (https://510kreport.com/company/msq-m2)
- Biolase Technology, Inc.: 1 (https://510kreport.com/company/biolase-technology)
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)
- Aerolase Medical Lasers, LLC: 1 (https://510kreport.com/company/aerolase-medical-lasers)
- Lameditech Co., Ltd.: 1 (https://510kreport.com/company/lameditech)

## Its most-cited devices
- K000023: Friendly Light ER:Yag Pulsed Laser (2000), cited by 3
- K033251: The Friendlylight ND: Yag Lasers (2004), cited by 2
- K013021: Lightlance Laser Skin Perforator (2002), cited by 1

## Recent decisions
- K033251: The Friendlylight ND: Yag Lasers (Mar 2, 2004)
- K013021: Lightlance Laser Skin Perforator (May 30, 2002)
- K000023: Friendly Light ER:Yag Pulsed Laser (Nov 6, 2000)

Source page: https://510kreport.com/company/innotech-usa