# Orion Diagnostica, Div. Orion Corp.

- Location (FDA's records): Espoo, FI
- FDA decisions: 4 (1995–2003): 4 510(k) clearances
- Product codes: DCK (2), LYR (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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 that cite its devices most
- Nichols Institute Diagnostics: 1 (https://510kreport.com/company/nichols-institute-diagnostics)

## Its most-cited devices
- K971537: Pyloriset Eia-G (68926) (1997), cited by 1

## Recent decisions
- K031607: Orion Diagnostica Quikread CRP Kit and Quikread CRP Control (Oct 10, 2003)
- K022176: Orion Diagnostica Ultrasensitive CRP Kit, Model 68025, & Orion Diagnostica Ultrasensitive CRP Control, Model 68257 (Dec 3, 2002)
- K971537: Pyloriset Eia-G (68926) (Jun 27, 1997)
- K942974: Pyloriset Dry (Apr 5, 1995)

Source page: https://510kreport.com/company/orion-diagnostica-div-orion