# Grifols USA, LLC

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 3 (2011–2012): 3 510(k) clearances
- Names in FDA's records: Grifols USA, LLC (2); Grifols USA, Inc. (1)
- Product codes: CFF (1), MVM (1), MST (1)
- Predicates its devices cite: 4 (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
- Grifols: 1 (https://510kreport.com/company/grifols)
- Scimedx Corp.: 1 (https://510kreport.com/company/scimedx)
- Aesku, Inc.: 1 (https://510kreport.com/company/aesku)
- Aesku Diagnostics: 1 (https://510kreport.com/company/aesku-diagnostics)

## Recent decisions
- K113377: Gliadin Iga and Gliadin Lga (Dec 14, 2012)
- K120169: Interlab Ife Test Using G 26 Ver. 2.0 Instrument (Aug 24, 2012)
- K102964: EU-TTG Iga  and EU-TTG Igg (Mar 7, 2011)

Source page: https://510kreport.com/company/grifols-usa