# Imediplus, Inc.

- Location (FDA's records): Chupei City, TW
- FDA decisions: 3 (2016–2018): 3 510(k) clearances
- Product codes: DQD (3)
- 510(k) review time since 2016: median 261 days, against 131 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (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
- 3M Company: 2 (https://510kreport.com/company/3m)

## Firms that cite its devices most
- Sound Land Corp.: 1 (https://510kreport.com/company/sound-land)

## Its most-cited devices
- K160023: Electronic Stethoscope DS301 (2016), cited by 2
- K173663: Electronic Stethoscope DS3011A (2018), cited by 1

## Recent decisions
- K182196: Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth (Sep 11, 2018)
- K173663: Electronic Stethoscope DS3011A (Aug 17, 2018)
- K160023: Electronic Stethoscope DS301 (Sep 30, 2016)

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