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Last updated: June 5, 2026
Back to directoryOxehealth Oxevision medical AI product profile
Contactless patient monitoring platform for inpatient mental health and ward-safety workflows, including Oxevision Sleep Device FDA clearance.
Clinical operations and revenue cycle
Best fit
Behavioral health and inpatient safety teams that need supervised room-level monitoring with explicit privacy, dignity, training, and escalation controls.
- Primary use case
- Contact-free vision-based ward monitoring, spot vital-sign observations, movement alerts, sleep reporting, and patient-safety workflow support
- Audience
- Inpatient behavioral health units, seclusion rooms, ward-safety leaders, nursing teams, and hospitals evaluating contactless patient observation
- Risk level
- High
- Pricing signal
- Enterprise implementation pricing is not public; request current hardware, software, training, support, and regional regulatory terms.
- Official sources
- 5 official sources
Compare within workflow: Clinical operations and revenue cycle · comparison shortlist · source index
Regulatory, privacy, evidence, and workflow lens
Product-specific review. These product-specific signals summarize what the cited sources imply before treating Oxehealth Oxevision as safe for a local clinical, operational, or research workflow.
| Regulatory / FDA | Separate Sleep, Vital Signs, Activity Tracker, Seclusion, and local observation workflows because FDA, UK/EU device status, CDSS status, version, and intended use can differ by module. |
|---|---|
| Privacy | Map camera/infrared data, live-view windows, clear-video requests, room context, reports, retention, access controls, patient notices, consent, ward policy, and support access before go-live. |
| Evidence | Validate the product in the target ward type and patient population, measuring false alerts, missed events, observation burden, nighttime disturbance, patient dignity, and incident-review quality. |
| Workflow | Best governed as supervised nursing and safety support, with trained users, explicit escalation rules, downtime plans, patient communication, and governance review of each ward deployment. |
Where Oxehealth Oxevision fits
Oxehealth training materials describe Oxevision as a contact-free, camera-based system for ward safety that provides alerts, readings, reports, and limited live video views; FDA records list Oxevision Sleep Device K233618 as a substantially equivalent neurology device, while Oxehealth IFU materials separate regulated Vital Signs software from Activity Tracker CDSS features.
Not for: General CCTV surveillance, autonomous patient safety decisions, multi-occupancy rooms, continuous vital-sign alarms, or use without patient notice and staff governance.
What to verify before using Oxehealth Oxevision
- Which Oxevision module is in scope: Vital Signs, Activity Tracker, Sleep, Seclusion, alerts, reports, or local digital-observation workflow.
- FDA or local regulatory status for the exact software version and intended use, including Oxevision Sleep Device K233618 and any non-device CDSS features.
- Room type, single-occupancy requirements, camera placement, video-viewing limits, patient notice, consent, privacy, retention, and dignity policy.
- Local performance for falls, self-harm risk, overnight checks, staff response, false alerts, missed events, patient experience, and incident-review workflow.
Source links
Use these links to confirm current claims, terms, regulatory status, pricing, and deployment requirements.
- www.oxehealth.academy / modules / what-is-oxevision
- www.oxehealth.academy / modules / what-does-oxevision-do
- www.oxehealth.academy / instructions-for-use
- www.accessdata.fda.gov / scripts / cdrh
- assets.website-files.com / 5f5678688f40811eed0fe944 / 62c3096344b6063ba7806edb_Oxehealth%20-%20Privacy%20Notice%20-%20Customer%20v6.pdf
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