# Dia-Screen Corp.

- Location (FDA's records): Edina, MN
- FDA decisions: 1 (1997–1997): 1 510(k) clearance
- Product codes: LJX (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Genesis Labs, Inc.: 3 (https://510kreport.com/company/genesis-labs)
- Bioscan Instruments, Inc.: 1 (https://510kreport.com/company/bioscan-instruments)

## Firms that cite its devices most
- Uridynamics, Inc.: 1 (https://510kreport.com/company/uridynamics)
- Ocusense, Inc.: 1 (https://510kreport.com/company/ocusense)

## Its most-cited devices
- K971976: Diascreen Reagent Strips (1997), cited by 2

## Recent decisions
- K971976: Diascreen Reagent Strips (Jun 17, 1997)

Source page: https://510kreport.com/company/dia-screen