fda_device_company_profile

shallow

io.github.pipeworx-io/fda-devices · Verify this server

Build a bounded FDA regulatory snapshot for one device company across 510(k), PMA, recalls, and MAUDE. Dataset name matching is imperfect and MAUDE counts are signals, not safety rates.

100.0/100

1 trials · measured 8 days ago

fda_device_company_profile scores 100.0/100 on Vouch's measured behaviour index, from 1 real invocation trials against io.github.pipeworx-io/fda-devices, measured 25 Aug 2026 under methodology v0.2.0. Every measured component scored 100.

Component breakdown

ComponentWeightValue
Reliability35%not applicable
Schema integrity25%100.0
Failure behaviour15%not applicable
Latency15%not applicable
Concurrency10%not applicable

Tool details

Transport
remote
Credential class
self-provisionable
Category
Health
Input schema
not declared
Output schema
not declared
Side-effect classification
unclassified

Score history

DayScoreTierMethodology
2026-08-25100.0shallowv0.2.0

Probe evidence

ProbeOutcomes
schema_integritypass: 1

Raw request/response logs are not archived yet — the outcome counts above are drawn directly from every recorded trial.

Embed this score

Available for every tool, scored or not — not a verification perk. Always links back to this page.

Vouch score: fda_device_company_profile
[![Vouch score](https://vouch.tools/api/tools/41acf6ac-7905-49d4-87f4-667beb497e65/badge.svg)](https://vouch.tools/tools/41acf6ac-7905-49d4-87f4-667beb497e65)
fda_device_company_profile — Vouch