# Oneday Biotech Co., Ltd.

- Location (FDA's records): Daegu, KR
- FDA decisions: 2 (2023–2024): 2 510(k) clearances
- Product codes: DZE (1), NHA (1)
- Predicates its devices cite: 3 (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 whose devices it cites most
- Dio Corporation: 2 (https://510kreport.com/company/dio)
- Izenimplant Co., Ltd.: 1 (https://510kreport.com/company/izenimplant)

## Firms that cite its devices most
- DIMPLO, Ltd.: 1 (https://510kreport.com/company/dimplo)

## Its most-cited devices
- K231753: Oneday Implant Abutment (2024), cited by 1

## Recent decisions
- K231753: Oneday Implant Abutment (Feb 21, 2024)
- K222946: Oneday Mini Implant System (Aug 23, 2023)

Source page: https://510kreport.com/company/oneday-biotech
