Data / Medical devices / Dilator, Vessel, For Percutaneous Catheterization

Dilator, Vessel, For Percutaneous Catheterization (DRE): 56 FDA-registered makers in 12 countries

56 establishments in 12 countries are registered with the FDA to make Dilator, Vessel, For Percutaneous Catheterization (product code DRE, Class 2, 21 CFR 870.1310). 34 of them have a 510(k) clearance or PMA approval on file and 6 have a recall event. The FDA has issued 105 510(k) clearances under this code, the latest on July 27, 2026, and lists 22 recall events (1 Class I). FDA data exported November 2, 2026.

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Product code

DRE

Device class

2

Regulation

870.1310

Medical specialty

Cardiovascular

Makers by country

Makers of Dilator, Vessel, For Percutaneous Catheterization

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Updated July 27, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.