# Topera, Inc.

- Location (FDA's records): St.Louis, MO
- FDA decisions: 7 (2011–2015): 7 510(k) clearances
- Product codes: DQK (5), MTD (2)
- Predicates its devices cite: 14 (11 its own); citations of its devices by later devices: 18 (11 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Boston Scientific Corp: 2 (https://510kreport.com/company/boston-scientific)
- Biosense Webster, Inc.: 1 (https://510kreport.com/company/biosense-webster)

## Firms that cite its devices most
- Abbott Electrophysiology: 7 (https://510kreport.com/company/abbott-electrophysiology)

## Its most-cited devices
- K130827: Firmap Catheter (2013), cited by 5
- K110878: Rhythmview (TM) (2011), cited by 5
- K123295: Rhythm View (2013), cited by 4
- K142901: RhythmView Workstation (2014), cited by 2
- K151245: Rhythm View Workstation (non-streaming, steaming option) (2015), cited by 2

## Recent decisions
- K151245: Rhythm View Workstation (non-streaming, steaming option) (Sep 15, 2015)
- K142901: RhythmView Workstation (Dec 19, 2014)
- K142182: Frimap Adapter Connector (Mac) (Sep 9, 2014)
- K133305: Rhythm View Workstation (Dec 16, 2013)
- K130827: Firmap Catheter (Oct 31, 2013)
- K123295: Rhythm View (Apr 24, 2013)
- K110878: Rhythmview (TM) (Sep 23, 2011)

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