# Osteon, Inc.

- Location (FDA's records): Wahiawa, HI
- FDA decisions: 2 (1985–1989): 2 510(k) clearances
- Product codes: KGI (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Lunar Corp.: 2 (https://510kreport.com/company/lunar)
- Norland Corp.: 1 (https://510kreport.com/company/norland)

## Its most-cited devices
- K891582: Modified Osteoanalyzer (# SPSHA110/220) (1989), cited by 3

## Recent decisions
- K891582: Modified Osteoanalyzer (# SPSHA110/220) (Sep 12, 1989)
- K843922: Osteon Bone Mineral Analyzer (Apr 2, 1985)

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