# Orthoaccel Technologies, Inc.

- Location (FDA's records): Bellaire, TX
- FDA decisions: 3 (2011–2016): 3 510(k) clearances
- Product codes: OYH (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 6 (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
- Myofunctional Research Corp. Pty., Ltd.: 1 (https://510kreport.com/company/myofunctional-research)
- Biolux Research, Ltd.: 1 (https://510kreport.com/company/biolux-research)

## Firms that cite its devices most
- Biolux Research, Ltd.: 2 (https://510kreport.com/company/biolux-research)
- Propel Orthodontics, LLC: 1 (https://510kreport.com/company/propel-orthodontics)
- Orthoaccel Technology, Inc.: 1 (https://510kreport.com/company/orthoaccel-technology)

## Its most-cited devices
- K110661: Acceledent (2011), cited by 2
- K130643: Acceledent Aura (2013), cited by 2
- K153048: AcceleDent Aura (2016), cited by 2

## Recent decisions
- K153048: AcceleDent Aura (Jul 8, 2016)
- K130643: Acceledent Aura (Apr 23, 2013)
- K110661: Acceledent (Nov 17, 2011)

Source page: https://510kreport.com/company/orthoaccel-technologies