# Xoft, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 6 (2005–2009): 6 510(k) clearances
- Product codes: JAD (5), IXI (1)
- Predicates its devices cite: 11 (2 its own); citations of its devices by later devices: 5 (2 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
- Proxima Therapeutics, Inc.: 3 (https://510kreport.com/company/proxima-therapeutics)
- Varian Medical Systems, Inc.: 2 (https://510kreport.com/company/varian-medical-systems)
- Arplay Medical S.A.: 1 (https://510kreport.com/company/arplay-medical)
- Nucletron Corp.: 1 (https://510kreport.com/company/nucletron)
- Photoelectron Corporation: 1 (https://510kreport.com/company/photoelectron)
- Varian Assoc., Inc.: 1 (https://510kreport.com/company/varian-assoc)

## Firms that cite its devices most
- Carl Zeiss Meditec, AG: 1 (https://510kreport.com/company/carl-zeiss-meditec)
- Icad, Inc.: 1 (https://510kreport.com/company/icad)
- Sensus Healthcare, Inc.: 1 (https://510kreport.com/company/sensus-healthcare)

## Its most-cited devices
- K050843: Axxent Electronic Brachytherapy System (2005), cited by 2
- K083734: Axxent Surface Applicator, Model 710257 (2009), cited by 1
- K090914: Axxent Balloon Applicator, Model AB2034, AB2045, AB2056, AB2057E, AB2067E (2009), cited by 1
- K072683: Axxent Electronic Brachytherapy System (2008), cited by 1

## Recent decisions
- K090914: Axxent Balloon Applicator, Model AB2034, AB2045, AB2056, AB2057E, AB2067E (Jul 16, 2009)
- K090417: Axxent Flexishield Mini (Jun 23, 2009)
- K083734: Axxent Surface Applicator, Model 710257 (Feb 11, 2009)
- K072616: Axxent Vaginal Applicator (May 9, 2008)
- K072683: Axxent Electronic Brachytherapy System (Feb 29, 2008)
- K050843: Axxent Electronic Brachytherapy System (Dec 22, 2005)

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