# Deep Blue Medical Advances, Inc.

- Location (FDA's records): Durham, NC
- FDA decisions: 4 (2020–2023): 4 510(k) clearances
- Product codes: FTL (4)
- 510(k) review time since 2016: median 84 days, against 84 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 7 (6 its own); citations of its devices by later devices: 6 (6 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
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K193144: T-Line Hernia Mesh (2020), cited by 3
- K221556: T-Line Hernia Mesh (2022), cited by 2
- K230227: T-Line Hernia Mesh (2023), cited by 1

## Recent decisions
- K232924: T-Line® Hernia Mesh (Oct 18, 2023)
- K230227: T-Line Hernia Mesh (Feb 23, 2023)
- K221556: T-Line Hernia Mesh (Nov 28, 2022)
- K193144: T-Line Hernia Mesh (Mar 30, 2020)

Source page: https://510kreport.com/company/deep-blue-medical-advances