# Osteoready, LLC

- Location (FDA's records): Seattle, WA
- FDA decisions: 2 (2015–2018): 2 510(k) clearances
- Product codes: NHA (1), DZE (1)
- Predicates its devices cite: 5 (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

## Firms whose devices it cites most
- A.B. Dental Devices, Ltd.: 2 (https://510kreport.com/company/ab-dental-devices)
- Clinical House Europe GmbH: 1 (https://510kreport.com/company/clinical-house-europe)
- Iq Implants, Ltd.: 1 (https://510kreport.com/company/iq-implants)
- Mis - Implant Technologies, Ltd.: 1 (https://510kreport.com/company/mis-implant-technologies)

## Recent decisions
- K173575: OsteoReady Dental Implant System (Aug 17, 2018)
- K151169: OsteoReady ZircoSeal Abutments (Oct 8, 2015)

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