# Bryan Corp.

- Location (FDA's records): Woburn, MA
- FDA decisions: 5 (1986–2000): 5 510(k) clearances
- Product codes: EOQ (1), NWA (1), HIH (1), MYU (1), HIF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Novatech SA: 1 (https://510kreport.com/company/novatech)
- Macropore Biosurgery, Inc.: 1 (https://510kreport.com/company/macropore-biosurgery)
- Vista Scientific, LLC: 1 (https://510kreport.com/company/vista-scientific)

## Its most-cited devices
- K002063: Biotrace, Model 1730 (2000), cited by 2
- K894380: Dumon Tracheobronchial Stent (1989), cited by 1

## Recent decisions
- K002063: Biotrace, Model 1730 (Aug 10, 2000)
- K913242: Microprocessed Controlled Laparoflator (Sep 25, 1992)
- K894380: Dumon Tracheobronchial Stent (Oct 24, 1989)
- K881249: Baggish, Hysteroscope (Jul 28, 1988)
- K854414: Dumon/Harrell (Mar 12, 1986)

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