# Global USA Distribution, LLC

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 4 (2008–2008): 4 510(k) clearances
- Product codes: GEX (4)
- Predicates its devices cite: 11 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Sciton, Inc: 3 (https://510kreport.com/company/sciton)
- Medical Laser Technologies, Ltd.: 1 (https://510kreport.com/company/medical-laser-technologies)
- Msq (M2), Ltd.: 1 (https://510kreport.com/company/msq-m2)
- New Star Lasers, Inc.: 1 (https://510kreport.com/company/new-star-lasers)
- Altus Medical, Inc.: 1 (https://510kreport.com/company/altus-medical)
- Cynosure, Inc.: 1 (https://510kreport.com/company/cynosure)
- Candela Corp.: 1 (https://510kreport.com/company/candela)
- Sandstone Medical Technologies, LLC: 1 (https://510kreport.com/company/sandstone-medical-technologies)

## Firms that cite its devices most
- Palomar Medical Technologies, Inc.: 1 (https://510kreport.com/company/palomar-medical-technologies)

## Its most-cited devices
- K082033: Nannolight Intense Pulsed Light System (2008), cited by 1

## Recent decisions
- K083272: Skinclear Q-Switched ND:Yag Laser (Dec 16, 2008)
- K082028: Laserpeel Soft-Met Modified Erbium Laser (Aug 8, 2008)
- K082033: Nannolight Intense Pulsed Light System (Jul 31, 2008)
- K080697: Skin Clear SRVH Long-Pulsed ND: Yag Laser (Apr 7, 2008)

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