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BodyMed

BOXOUT, LLC · Model ZZAIF450 · UDI-DI 00815802010870

LIH Prescription
10
510(k) clearances
45
Adverse events
0
Recalls
47
Facilities

Description

BODYMED ANALOG DUAL CHANNEL INTERFERENTIAL UNIT

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.