# Corindus, Inc.

- Location (FDA's records): Waltham, MA
- FDA decisions: 9 (2012–2022): 9 510(k) clearances
- Product codes: DXX (9)
- 510(k) review time since 2016: median 76 days, against 76 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 15 (11 its own); citations of its devices by later devices: 11 (11 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
- Hansen Medical, Inc.: 3 (https://510kreport.com/company/hansen-medical)
- Stereotaxis, Inc.: 1 (https://510kreport.com/company/stereotaxis)

## Its most-cited devices
- K120834: Corpath 200 System (2012), cited by 3
- K160121: CorPath GRX System (2016), cited by 2
- K150892: CorPath 200 System (2015), cited by 2
- K202275: CorPath GRX System (2020), cited by 1
- K173806: CorPath GRX System (2018), cited by 1
- K173288: CorPath GRX System (2018), cited by 1

## Recent decisions
- K221464: CorPath GRX System (Jul 27, 2022)
- K202275: CorPath GRX System (Dec 11, 2020)
- K180517: CorPath GRX System (Mar 29, 2018)
- K173806: CorPath GRX System (Mar 1, 2018)
- K173288: CorPath GRX System (Feb 15, 2018)
- K160121: CorPath GRX System (Oct 27, 2016)
- K152999: CorPath 200 System (Mar 18, 2016)
- K150892: CorPath 200 System (Oct 2, 2015)

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