# Disco, Inc.

- Location (FDA's records): West Linn, OR
- FDA decisions: 2 (1991–1993): 2 510(k) clearances
- Product codes: DXC (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
- Anlam Corp.: 1 (https://510kreport.com/company/anlam)

## Its most-cited devices
- K923085: Quicklamp System (1993), cited by 1

## Recent decisions
- K923085: Quicklamp System (Feb 12, 1993)
- K914149: Femoral Artery Pressure Pad/Disk (Dec 13, 1991)

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