Data / Medical devices / Dam, Rubber

Dam, Rubber (EIE): 77 FDA-registered makers in 17 countries

77 establishments in 17 countries are registered with the FDA to make Dam, Rubber (product code EIE, Class 1, 21 CFR 872.6300). 10 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 33 510(k) clearances under this code, the latest on May 3, 2019, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

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Product code

EIE

Device class

1

Regulation

872.6300

Medical specialty

Dental

Makers by country

Makers of Dam, Rubber

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 May 3, 2019. 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.