# Aesthera Corporation

- Location (FDA's records): Concord, CA
- FDA decisions: 3 (2005–2009): 3 510(k) clearances
- Product codes: GEX (3)
- Predicates its devices cite: 17 (2 its own); citations of its devices by later devices: 5 (2 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
- Radiancy (Israel), Ltd.: 6 (https://510kreport.com/company/radiancy-israel)
- Palomar Medical Technologies, Inc.: 3 (https://510kreport.com/company/palomar-medical-technologies)
- Radiancy, Ltd.: 2 (https://510kreport.com/company/radiancy)
- Palomar Medical Products, Inc.: 2 (https://510kreport.com/company/palomar-medical-products)
- Novalis Medical, LLC: 1 (https://510kreport.com/company/novalis-medical)
- Palomar: 1 (https://510kreport.com/company/palomar)

## Firms that cite its devices most
- Theravant Corporation: 1 (https://510kreport.com/company/theravant)
- Inolase 2002, Ltd.: 1 (https://510kreport.com/company/inolase-2002)
- Solta Medical, Inc.: 1 (https://510kreport.com/company/solta-medical)

## Its most-cited devices
- K083730: Isolaz (2009), cited by 2
- K041554: Aip Intense Pulsed Light System (2005), cited by 2
- K062048: Aesthera Photopneumatic (PPX) System (2006), cited by 1

## Recent decisions
- K083730: Isolaz (Jan 9, 2009)
- K062048: Aesthera Photopneumatic (PPX) System (Sep 7, 2006)
- K041554: Aip Intense Pulsed Light System (Apr 27, 2005)

Source page: https://510kreport.com/company/aesthera