# Televere Systems

- Location (FDA's records): Arnold, MD
- FDA decisions: 6 (2006–2018): 6 510(k) clearances
- Names in FDA's records: Televere Systems (4); Televere Systems, Inc. (2)
- Product codes: MQB (2), LLZ (2), KPR (1), MUH (1)
- 510(k) review time since 2016: median 29 days, against 30 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 10 (3 its own); citations of its devices by later devices: 9 (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
- Eaglesoft, A Patterson Co.: 2 (https://510kreport.com/company/eaglesoft-a-patterson)
- Tau Corp.: 2 (https://510kreport.com/company/tau)
- Arquilla, Inc. Dba X-Cel X-Ray Corporation: 1 (https://510kreport.com/company/arquilla-dba-x-cel-x-ray)
- Trident S.R.L: 1 (https://510kreport.com/company/trident)
- Viztek, LLC: 1 (https://510kreport.com/company/viztek)

## Firms that cite its devices most
- American Dental Partners, Inc.: 2 (https://510kreport.com/company/american-dental-partners)
- Jpi Healthcare Solutions, Inc.: 1 (https://510kreport.com/company/jpi-healthcare-solutions)
- Planmeca Oy: 1 (https://510kreport.com/company/planmeca)
- Raster Builders, Inc.: 1 (https://510kreport.com/company/raster-builders)
- Durr Dental SE: 1 (https://510kreport.com/company/durr-dental)

## Its most-cited devices
- K061035: Tigerview Professional (2006), cited by 5
- K082623: Visix Imaging (2009), cited by 2
- K170975: Televere Digital Imaging System (2017), cited by 2

## Recent decisions
- K181358: Televere Digital Dental Imaging System (Jun 20, 2018)
- K180765: Televere Podiatry X-Ray System HF (Apr 20, 2018)
- K172124: Televere Podiatry Digital Imaging System (Nov 9, 2017)
- K170975: Televere Digital Imaging System (May 1, 2017)
- K082623: Visix Imaging (Feb 25, 2009)
- K061035: Tigerview Professional (Jun 5, 2006)

Source page: https://510kreport.com/company/televere-systems