# Intermedic Arfran, SA

- Location (FDA's records): Meza, AZ
- FDA decisions: 2 (2006–2009): 2 510(k) clearances
- Product codes: GEX (2)
- Predicates its devices cite: 17 (1 its own); citations of its devices by later devices: 8 (1 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
- Syneron Medical, Ltd.: 6 (https://510kreport.com/company/syneron-medical)
- Biolitec, Inc.: 3 (https://510kreport.com/company/biolitec)
- Dornier Medtech America, Inc.: 2 (https://510kreport.com/company/dornier-medtech-america)
- Dornier Surgical Products, Inc.: 2 (https://510kreport.com/company/dornier-surgical-products)
- Surgical Laser Technologies, Inc.: 1 (https://510kreport.com/company/surgical-laser-technologies)
- Photo Medex, Inc.: 1 (https://510kreport.com/company/photo-medex)
- Ceram Optec, Inc.: 1 (https://510kreport.com/company/ceram-optec)

## Firms that cite its devices most
- Biolitec, Inc.: 3 (https://510kreport.com/company/biolitec)
- Quanta System Spa: 2 (https://510kreport.com/company/quanta-system)
- Litecure, LLC: 1 (https://510kreport.com/company/litecure)
- Lasering S.R.L.: 1 (https://510kreport.com/company/lasering)

## Its most-cited devices
- K053540: Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories That Are Used with Them to Deliver Laser Ene (2006), cited by 8

## Recent decisions
- K091323: Modified Intermedic Diode Laser 980NM System (Multidiode SST 200) (Jun 4, 2009)
- K053540: Intermedic Diode Laser Family 810NM and 980NM (and the Delivery Accessories That Are Used with Them to Deliver Laser Ene (Sep 6, 2006)

Source page: https://510kreport.com/company/intermedic-arfran