Devigion
Devigion
FDA MAUDE
EUDAMED
PARD (UK)
TGA DAEN (AU)
Health Canada
GUDID
MDALL
PMDA (JP)

Medical Device Post-Market Surveillance Unified Platform

Aggregate Reports · Comparative Reports · Trends Analysis · Verbatim Access · Cross-Device Safety Signals

10M+

Adverse Events Analyzed

20+

Years of Historical Data

50+

Countries Covered

All

Device Classes

Core Capabilities

Pharmacovigilance, Reinvented

Stop searching database by database, device by device. Devigion transforms fragmented safety data from multiple regulatory agencies into structured, actionable intelligence.

Cross-Device Signal Detection

Track adverse event trends across materials, categories, and manufacturers. Identify if a defect in your device is isolated — or affects all similar devices industry-wide.

Competitive Intelligence

Compare your safety profile against the entire market. Class effects vs. device-specific signals — quantified across all regulatory databases.

Regulatory Compliance

Pre-built templates for PSUR, MDR, Post-Market Surveillance and 510(k) reports. Auto-generated compliance documents ready for submission.

Pricing

Choose Your Plan

From individual researchers to enterprise pharmacovigilance teams. Start free, scale when you need to.

Researcher
Free

For academics and individual clinicians exploring device safety data across all categories.

Overview dashboard

Basic trend analysis

5Y historical data

Export up to 100 records

⭐ Most Popular
Professional
$1,900/month

For manufacturers, pharmacovigilance teams, and regulatory affairs professionals.

Full dashboard suite

All historical data

Cross-device comparison

Material & problem drilldown

Unlimited exports

AI-powered query engine

Enterprise
Custom

For multi-product portfolios and health systems needing custom integrations.

Everything in Professional

Custom compliance reports

Internal data integration

Dedicated PV analyst support

SLA & priority support

SSO & team management

Devigion
Devigion

Medical Device Safety Intelligence for manufacturers, pharmacovigilance teams, clinics, researchers, and regulators.

Data sourced from FDA MAUDE, Health Canada, EUDAMED, WHO MeDevIs, TGA, PARD via public APIs. This platform is not affiliated with or endorsed by any regulatory agency. Medical device reports are subject to limitations including incomplete, inaccurate, or biased data. Do not use this platform as the sole basis for clinical or regulatory decisions.
© 2026 Devigion. All rights reserved.