# Bellus Medical, LLC

- Location (FDA's records): Dallas, TX
- FDA decisions: 1 (2018–2018): 1 De Novo grant
- Product codes: QAI (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Mt. Derm GmbH: 2 (https://510kreport.com/company/mt-derm)
- Equipmed USA, LLC: 1 (https://510kreport.com/company/equipmed-usa)
- Refine USA, LLC: 1 (https://510kreport.com/company/refine-usa)
- Eclipse Medcorp, LLC: 1 (https://510kreport.com/company/eclipse-medcorp)
- Bomtech Electronics Co., Ltd.: 1 (https://510kreport.com/company/bomtech-electronics)
- Esthetic Education, LLC: 1 (https://510kreport.com/company/esthetic-education)
- Dermaroller GmbH: 1 (https://510kreport.com/company/dermaroller)
- Guangzhou Ekai Electronic Technology Co., Ltd.: 1 (https://510kreport.com/company/guangzhou-ekai-electronic-technology)

## Its most-cited devices
- DEN160029: SkinPen Precision System (2018), cited by 9

## Recent decisions
- DEN160029: SkinPen Precision System (Mar 1, 2018)

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