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End-UseCategory 2
U.S. imports of medicinal equipment (End-Use 21610) totaled $5.4B in July 2026, traded with 143 countries.
Importers of Medicinal Equipment paid $333.5M in duties in July 2026 — an effective duty rate of 11% on $2.9B in dutiable value, based on actual customs collections rather than the published tariff schedule.
Last updated: July 2026 dataImported medicinal equipment — including MRI systems, ultrasound devices, infusion pumps, and surgical tools — must comply with FDA device regulations before entering US commerce, with the applicable pathway (510(k), PMA, or De Novo) determined by device classification and risk level. Foreign manufacturers must be registered with FDA and list their devices, and shipments are subject to FDA examination at the port of entry; detained shipments can result in costly delays or refusal of admission. Section 301 tariffs apply to certain medical device imports of Chinese origin, adding a duty-cost dimension that procurement teams must factor into total landed cost analysis.
AI-written summary of the official U.S. Census Bureau trade figures on this page — verify before relying on it.
190.0K shipments/mo
End-Use codes describe different products on the import and export sides. Cross-direction exports are not shown for this slug.
Commodity 7 of 32 in category 2
Commodity 21610 · $5.4B of $148.5B
FDA may detain a shipment if the foreign manufacturer is not registered, the device is not listed, the product appears adulterated or misbranded, or prior import alerts are in place against the manufacturer or product. Importers can reduce detention risk by verifying manufacturer registration status in FDA's database before placing orders and ensuring all labeling meets US requirements.
Importers face a dual compliance burden: FDA admissibility review and elevated duty costs under Section 301 for Chinese-origin goods. Some importers have pursued first-sale valuation or tariff engineering strategies to manage duty exposure, while others have shifted sourcing to non-Section 301 countries. Any sourcing change requires re-evaluation of FDA establishment registration and device listing for the new manufacturer. Consult a licensed customs broker and regulatory counsel to coordinate both compliance tracks.
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Imports · July 2026
origin
customs district
Census does not publish district detail for this classification system.
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Census does not publish state detail for this classification system.
entry
Census does not publish port detail for this classification system.
ImportsExports
Imports
$5.4BYoY · Pro
12-mo low · imports
YoY · ProThrough July 2026. Source: U.S. Census Bureau.