inforMED
KQXClass I

Goniometer, Ac-powered

Orthopedic · 21 CFR 888.1500

MDR events0All time
Recalls0All time
Registered firms48Currently listed
510(k) clearances33All time

Recent MDR events

0 adverse event reports on file

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No MDR events on file for this product code.

Event type breakdown

No data available.

Most-reported manufacturers

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No data available.

Recalls

0 recall events for this product code

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No recalls on file for this product code.