# Ortholution Co., Ltd.

- Location (FDA's records): Dunwoody, GA
- FDA decisions: 3 (2005–2008): 3 510(k) clearances
- Product codes: DZE (3)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 6 (3 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
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Osteomed LP: 1 (https://510kreport.com/company/osteomed)

## Firms that cite its devices most
- Micerium S.P.A.: 1 (https://510kreport.com/company/micerium)
- Odontit S.A.: 1 (https://510kreport.com/company/odontit)
- Jjgc Industria E Comercio DE Materiais Dentarios S: 1 (https://510kreport.com/company/jjgc-industria-e-comercio-de-materiais-dentarios-s)

## Its most-cited devices
- K050568: Orlus Mini Screw (2005), cited by 4
- K082838: Orlus Mini Screw (2008), cited by 1
- K052968: Modification to: Orlus Mini Screw (2006), cited by 1

## Recent decisions
- K082838: Orlus Mini Screw (Nov 25, 2008)
- K052968: Modification to: Orlus Mini Screw (Sep 8, 2006)
- K050568: Orlus Mini Screw (Jun 1, 2005)

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