Data / Medical devices / Stethoscope, Manual

Stethoscope, Manual (LDE): 105 FDA-registered makers in 10 countries

105 establishments in 10 countries are registered with the FDA to make Stethoscope, Manual (product code LDE, Class 1, 21 CFR 870.1875). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 28 510(k) clearances under this code, the latest on December 8, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

LDE

Device class

1

Regulation

870.1875

Medical specialty

Cardiovascular

Makers by country

Makers of Stethoscope, Manual

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 December 8, 1994. 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.