# Orion Corp.

- Location (FDA's records): 20101 Turku, FI
- FDA decisions: 21 (1985–1992): 21 510(k) clearances
- Product codes: LQN (4), JSI (3), IZH (3), MSJ (2), LJP (2), DCN (1), JJJ (1), IZF (1), DDR (1), DCF (1), LIQ (1), LJC (1)
- 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
- Orion Corporation Soredex: 1 (https://510kreport.com/company/orion-soredex)

## Its most-cited devices
- K884650: Resubmitted Scanora (1989), cited by 1

## Recent decisions
- K912391: Rubalex, Modification (May 4, 1992)
- K901637: Resubmitted Modified Rubalex (Apr 26, 1990)
- K884650: Resubmitted Scanora (Mar 16, 1989)
- K890199: Dentocult SM-Strip Mutans (Mar 2, 1989)
- K881505: Mamex DC MG11 (Jun 10, 1988)
- K881506: Mamex DC Mag MG12 (Jun 10, 1988)
- K874040: Mamex DC S  SL10/MG14 (Nov 23, 1987)
- K872744: Modified Chlamyset Antigen (Sep 22, 1987)

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