# Curatia Medical Co.

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 3 (2017–2022): 3 510(k) clearances
- Names in FDA's records: Curatia Medical Co. (2); Curatia Medical (1)
- Product codes: DQY (1), DYB (1), LIT (1)
- 510(k) review time since 2016: median 78 days, against 106 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (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

## Firms whose devices it cites most
- Cordis Corp.: 1 (https://510kreport.com/company/cordis)
- Terumo Medical Corp.: 1 (https://510kreport.com/company/terumo-medical)
- Bard Peripheral Vascular, Inc.: 1 (https://510kreport.com/company/bard-peripheral-vascular)

## Recent decisions
- K220604: EXTesia Introducer Sheath Set (Apr 27, 2022)
- K180797: Xcess Guiding Catheter (Dec 14, 2018)
- K171290: Vela RX PTA Balloon Dilatation Catheter (Jul 19, 2017)

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