# Bryan Medical, Inc.

- Location (FDA's records): Cincinnati, OH
- FDA decisions: 4 (2015–2026): 4 510(k) clearances
- Product codes: BTR (3), KTI (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 3 (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
- Xomed, Inc.: 1 (https://510kreport.com/company/xomed)
- Acclarent, Inc.: 1 (https://510kreport.com/company/acclarent)
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)

## Firms that cite its devices most
- M/S Meril Life Sciences Pvt., Ltd.: 1 (https://510kreport.com/company/m-s-meril-life-sciences-pvt)

## Its most-cited devices
- K200761: Tenax Laser Resistant Endotracheal Tube (2020), cited by 1
- K213028: Tenax Laser Resistant Endotracheal Tube (2021), cited by 1
- K150951: aeris Balloon Dialation Catheter (2015), cited by 1

## Recent decisions
- K251794: Tenax® Laser Resistant Endotracheal Tube (Sep 3, 2026)
- K213028: Tenax Laser Resistant Endotracheal Tube (Oct 21, 2021)
- K200761: Tenax Laser Resistant Endotracheal Tube (Nov 25, 2020)
- K150951: aeris Balloon Dialation Catheter (Jun 25, 2015)

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