# Rodo Medical, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 3 (2016–2020): 3 510(k) clearances
- Product codes: NHA (3)
- 510(k) review time since 2016: median 93 days, against 200 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 2 (2 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
- Astra Tech, Inc.: 1 (https://510kreport.com/company/astra-tech)
- Biomet 3i, Inc.: 1 (https://510kreport.com/company/biomet-3i)

## Its most-cited devices
- K160786: RODO Abutment System (2016), cited by 2

## Recent decisions
- K193274: Rodo Abutment System (Feb 27, 2020)
- K180609: Rodo Smilekey (May 23, 2018)
- K160786: RODO Abutment System (Nov 21, 2016)

Source page: https://510kreport.com/company/rodo-medical