# Bioform Medical, Inc.

- Location (FDA's records): San Mateo, CA
- FDA decisions: 3 (2006–2008): 3 510(k) clearances
- Product codes: MIX (2), GXD (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 5 (1 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
- Bioform, Inc.: 2 (https://510kreport.com/company/bioform)
- Aci, Inc.: 1 (https://510kreport.com/company/aci)
- Radionics, Inc.: 1 (https://510kreport.com/company/radionics)

## Firms that cite its devices most
- Cytophil, Inc.: 3 (https://510kreport.com/company/cytophil)
- Sofregen Medical, Inc.: 1 (https://510kreport.com/company/sofregen-medical)

## Its most-cited devices
- K070090: Radiesse Laryngeal Implant (2007), cited by 4
- K060815: Juliesse Injectable Laryngeal Augmentation Implant (2006), cited by 1

## Recent decisions
- K081729: Modification to GFX Nerve Ablation System (Aug 7, 2008)
- K070090: Radiesse Laryngeal Implant (Mar 1, 2007)
- K060815: Juliesse Injectable Laryngeal Augmentation Implant (Apr 18, 2006)

Source page: https://510kreport.com/company/bioform-medical