# Optus, Inc.

- Location (FDA's records): Denver, CO
- FDA decisions: 10 (1994–1996): 10 510(k) clearances
- Product codes: GCJ (2), HRX (2), EOB (1), CCW (1), FAJ (1), EOQ (1), ERA (1), HIH (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
- Acclarent, Inc.: 1 (https://510kreport.com/company/acclarent)

## Its most-cited devices
- K944656: Optus Sinuscopes and Accessories (1995), cited by 1

## Recent decisions
- K945264: Optus Otoscopes (Feb 2, 1996)
- K953913: Optus Arthroscope & Mini-Arthroscope Accessories (Jan 22, 1996)
- K945268: Optus Bronchoscopes (Dec 21, 1995)
- K945265: Optus Hysteroscopes and Contact Hysteroscopes (Sep 12, 1995)
- K945262: Optus Cystoscopes and Pediatric Cystoscopes (May 26, 1995)
- K945267: Optus Arthroscopes and Mini-Arthroscopes (May 23, 1995)
- K945266: Optus Laparoscopes and Operating Laparoscopes (Feb 23, 1995)
- K944656: Optus Sinuscopes and Accessories (Jan 26, 1995)

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