# Prosomnus Sleep Technologies

- Location (FDA's records): Pleasanton, CA
- FDA decisions: 3 (2020–2026): 3 510(k) clearances
- Names in FDA's records: Prosomnus Sleep Technologies (2); Prosomnus Sleep Technologies, Inc. (1)
- Product codes: LRK (2), PLC (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 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
- Microdental, Inc.: 2 (https://510kreport.com/company/microdental)
- Sketchpad Innovations, LLC: 1 (https://510kreport.com/company/sketchpad-innovations)

## Firms that cite its devices most
- Achaemenid, LLC: 1 (https://510kreport.com/company/achaemenid)

## Its most-cited devices
- K252765: ProSomnus RPMO2 OSA Device (RPMO2 OSA) (2026), cited by 1
- K202529: ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring (2020), cited by 1

## Recent decisions
- K252765: ProSomnus RPMO2 OSA Device (RPMO2 OSA) (Apr 6, 2026)
- K221889: ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring (Oct 6, 2022)
- K202529: ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring (Nov 20, 2020)

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