# Smartmissimo Technologies Pte, Ltd.

- Location (FDA's records): Singapore, SG
- FDA decisions: 5 (2015–2021): 5 510(k) clearances
- Product codes: IPF (3), NGX (2)
- 510(k) review time since 2016: median 99 days, against 98 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 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
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)

## Firms that cite its devices most
- Motive Health, Inc.: 1 (https://510kreport.com/company/motive-health)
- Medical Currents, Ltd.: 1 (https://510kreport.com/company/medical-currents)

## Its most-cited devices
- K150078: PowerDot (R) PD-01 Muscle Stimulator (with PowerDot (R) Mobile Application) (2015), cited by 2

## Recent decisions
- K210938: PowerDot PD-01MT2 Muscle Stimulator (Jul 30, 2021)
- K210269: PowerDot PD-01MT2 Muscle Stimulator (Feb 23, 2021)
- K181759: PowerDot PD-01MT (Nov 9, 2018)
- K172876: PowerDot PD-01M (Dec 4, 2017)
- K150078: PowerDot (R) PD-01 Muscle Stimulator (with PowerDot (R) Mobile Application) (Sep 30, 2015)

Source page: https://510kreport.com/company/smartmissimo-technologies