# The Traumafuse Co.

- Location (FDA's records): Allentown, PA
- FDA decisions: 4 (1989–1990): 4 510(k) clearances
- Product codes: BTO (1), DTN (1), DWE (1), BTR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K895162: Traumafuse Trach Shield (Jan 9, 1990)
- K894721: Traumafuse Perfusion Pressure Relief Valve (Oct 20, 1989)
- K895132: Connell-Stephens Endo Aness Tube (Oct 13, 1989)
- K890077: Traumafuse Rapid Infusion Device (Apr 3, 1989)

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