# Tactile Systems Technology, Inc. (Dba Tactile Medical)

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 3 (2016–2020): 3 510(k) clearances
- Product codes: JOW (2), PPS (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 6 (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
- Tactile Systems Technology, Inc.: 3 (https://510kreport.com/company/tactile-systems-technology)
- Mego Afek AC, Ltd.: 1 (https://510kreport.com/company/mego-afek-ac)

## Firms that cite its devices most
- Koya Medical, Inc.: 2 (https://510kreport.com/company/koya-medical)
- Koya, Inc.: 1 (https://510kreport.com/company/koya)
- Tactile Medical: 1 (https://510kreport.com/company/tactile-medical)

## Its most-cited devices
- K203178: Flexitouch Plus System (2020), cited by 3
- K170216: Flexitouch System (2017), cited by 2
- K153311: Flexitouch System (2016), cited by 1

## Recent decisions
- K203178: Flexitouch Plus System (Dec 20, 2020)
- K170216: Flexitouch System (May 26, 2017)
- K153311: Flexitouch System (Sep 14, 2016)

Source page: https://510kreport.com/company/tactile-systems-technology-dba-tactile-medical