# B. Braun Interventional Systems, Inc.

- Location (FDA's records): Bethlehem, PA
- FDA decisions: 3 (2013–2017): 3 510(k) clearances
- Product codes: LOX (1), LJT (1), DTK (1)
- Predicates its devices cite: 13 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- B.Braun Medical, Inc.: 4 (https://510kreport.com/company/b-braun-medical)
- Boston Scientific Corp: 3 (https://510kreport.com/company/boston-scientific)
- B. Braun of America, Inc.: 3 (https://510kreport.com/company/b-braun-of-america)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- B. Braun/Mcgaw: 1 (https://510kreport.com/company/b-braun-mcgaw)
- Bbraun: 1 (https://510kreport.com/company/bbraun)

## Firms that cite its devices most
- Novate Medical, Ltd.: 1 (https://510kreport.com/company/novate-medical)

## Its most-cited devices
- K152765: Venatech Convertible Vena Cava Filter System (2016), cited by 1

## Recent decisions
- K162625: SeQuent Neo Percutaneous Transluminal Coronary Angioplasty (PTCA) Balloon Catheters (Jun 12, 2017)
- K152765: Venatech Convertible Vena Cava Filter System (Feb 26, 2016)
- K130576: Celsite Implantable Access Port Systems (Apr 2, 2013)

Source page: https://510kreport.com/company/b-braun-interventional-systems