# Ostex Intl., Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 5 (1995–2001): 5 510(k) clearances
- Product codes: JMM (5)
- 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
- Ortho-Clinical Diagnostics, Inc.: 1 (https://510kreport.com/company/ortho-clinical-diagnostics)

## Its most-cited devices
- K980518: Osteomark (1998), cited by 1

## Recent decisions
- K011052: Osteomark NTX Point of Care Prescription Home Use (Jul 30, 2001)
- K983457: Osteomark NTX Serum Eia (Feb 2, 1999)
- K980518: Osteomark (Mar 6, 1998)
- K961562: Osteomark (Jul 11, 1996)
- K945946: Osteomark (R) (May 8, 1995)

Source page: https://510kreport.com/company/ostex-intl