# Ortho Pared Instruments, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1981–1983): 4 510(k) clearances
- Product codes: HRX (1), HTZ (1), GDL (1), HTW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K831772: Guillotine Blade (Jul 7, 1983)
- K820225: Meniscus Extractor (Feb 4, 1982)
- K820226: Universall Drill Guide (Feb 4, 1982)
- K812566: Universal Suture Passer (Nov 10, 1981)

Source page: https://510kreport.com/company/ortho-pared-instruments