# Dentos, Inc.

- Location (FDA's records): Ann Arbor, MI
- FDA decisions: 2 (2006–2019): 2 510(k) clearances
- Product codes: DZE (1), OAT (1)
- Predicates its devices cite: 3 (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 whose devices it cites most
- Dentaurum: 1 (https://510kreport.com/company/dentaurum)
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Imtec Corp.: 1 (https://510kreport.com/company/imtec)

## Firms that cite its devices most
- Leone S.P.A.: 1 (https://510kreport.com/company/leone)
- Creekside Orthodontics: 1 (https://510kreport.com/company/creekside-orthodontics)
- T.O.a.D.S., LLC: 1 (https://510kreport.com/company/toads)

## Its most-cited devices
- K060126: Absoanchor Microimplant (2006), cited by 3

## Recent decisions
- K181142: Absoanchor Microimplant (Feb 5, 2019)
- K060126: Absoanchor Microimplant (May 16, 2006)

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