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BODYTRACE, INC

No linked events in the loaded window. · aggregated across 2 source records

Scorecard
Events per device across the 11-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
11 device records · ordered by linked event volume.
BrandModelProduct codesPrimary DILinked events
BodyTraceBT007BFRIB726BT007B00
BodyTraceBT105DXNB726BT10500
BodyTraceBT007AFRIB726BT007A00
BodyTraceBT006FRIB726BT00600
BodyTraceBT005FRIB726BT00500
BodyTraceBT106DXNB726BT10600
BodyTraceBT104DXNB726BT10400
OmadaBT104ODXNB726BT104O00
OmadaBT005FRIB726BT005O00
OmadaBT105ODXNB726BT105O00
VidaBT005FRIB726BT005V00
Facilities
Registered establishments with their latest FDA inspection outcome.
FEINameLocationLast inspectionWatch
3011912849BODYTRACESan Jose, CA, US