KATENA PRODUCTS, INC.
18 adverse events · 3 inspections · aggregated across 3 source records
Scorecard
Events per device across the 4,376-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.
MAUDE reports per device
0.001 ▼
3 in the last 12 months
Higher volume than 84% of companies with 10+ devices
Recalls per device
0 →
0 in the last 12 months
Higher volume than 97% of companies with 10+ devices
These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.
Devices
4,376 device records · ordered by linked event volume.
Showing 1–30 of 4,376Next →
Facilities
Registered establishments with their latest FDA inspection outcome.
No registered facilities linked.