Observed arrival · 2026-09-24
Clearance Wire watches FDA device data
A paid monitoring service for medical-device product codes, with alerts for clearances, predicate recalls, and adverse-event spikes.
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$Paid
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✦Pretty
●Pro
◎Niche
◉Human
⚑Risk
ƒJS
- For
- Regulatory consultants and medical-device strategy teams
- Worth noticing
- The homepage says one seat can cover every client; it also notes that FDA 510(k) records may appear about a week after the decision date.
Field notes
The workflow starts with FDA product codes selected by the user, then the service says it connects clearance records to predicates, recalls, and adverse-event data. Its example alert includes a 510(k) identifier and a link to the FDA source. The FAQ notes that 510(k) records can lag decision dates by about a week and reproduces openFDA’s warning that results are unvalidated.
Observed signals
Read the marks
Editorial observations of this landing page, not a rating.
○OpenPublic substance visible
⊠LoginAccess appeared gated
$PaidCommerce or pricing visible
✦PrettyNotable craft visible
◎NicheUnusually specific use
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