# Iotamotion, Inc.

- Location (FDA's records): Iowa City, IA
- FDA decisions: 2 (2021–2026): 1 510(k) clearance and 1 De Novo grant
- Product codes: QQH (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- DEN190055: iotaSOFT Insertion System - Drive Unit, Controller and Accessories (2021), cited by 1

## Recent decisions
- K252339: iotaSOFT® Insertion System (Jan 9, 2026)
- DEN190055: iotaSOFT Insertion System - Drive Unit, Controller and Accessories (Oct 1, 2021)

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