Data / Medical devices / Mouthpiece, Saliva Ejector

Mouthpiece, Saliva Ejector (DYN): 109 FDA-registered makers in 15 countries

109 establishments in 15 countries are registered with the FDA to make Mouthpiece, Saliva Ejector (product code DYN, Class 1, 21 CFR 872.6640). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 18 510(k) clearances under this code, the latest on August 17, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

DYN

Device class

1

Regulation

872.6640

Medical specialty

Dental

Makers by country

Makers of Mouthpiece, Saliva Ejector

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 August 17, 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.