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A PLUS INTERNATIONAL INC.

8 inspections · 5 adverse events · 2 clearances · aggregated across 2 source records

Scorecard
Events per device across the 377-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.

MAUDE reports per device

0

0 in the last 12 months

Higher volume than 83% 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
377 device records · ordered by linked event volume.
BrandModelProduct codesPrimary DILinked events
A Plus1GDY006835348601132
A Plus1FRL006835348200251
A Plus1NAB006835348404500
A Plus1NAB006835348404810
A Plus1NAB006835348405280
A Plus1NAB006835348404670
A Plus1EFQ006835348500770
A Plus1GDY006835348700200
A Plus1EFQ006835348500840
A Plus1NAB006835348404980
A Plus1EFQ006835348500150
A Plus1EFQ006835348500220
A Plus1NAB006835348405420
A Plus1EFQ006835348700820
A Plus1GDY006835348700440
A Plus1KKX006835342102390
A Plus1GDY006835348602430
A Plus1GDY006835348602290
A Plus1EFQ006835348601990
A Plus1GDY006835348601820
A Plus1GDY006835348601680
A Plus1GDY006835348601510
A Plus1GDY006835348601440
A Plus1GDY006835348601370
A Plus1GDY006835348600900
A Plus1GDY006835348600830
A Plus1EFQ006835348501380
A Plus1GDY006835348600140
A Plus1EFQ006835348500910
A Plus1NAB006835348405110
Showing 1–30 of 377Next →
Facilities
Registered establishments with their latest FDA inspection outcome.
FEINameLocationLast inspectionWatch
2083545A PLUS INTERNATIONAL, INCCHINO, CA, USVAI