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Data / Medical devices / Mouthpiece, Saliva Ejector / United States

FDA-registered makers of Mouthpiece, Saliva Ejector in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Mouthpiece, Saliva Ejector (product code DYN). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Mouthpiece, Saliva Ejector
Product code
DYN
Country
United States

Makers of Mouthpiece, Saliva Ejector in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A-dec, Inc.Newberg, OR, United StatesManufacturer0000api.fda.gov
Ascentcare Dental ProductsGrand Haven, MI, United StatesManufacturer0000api.fda.gov
Beaverstate Dental, Inc.Newberg, OR, United StatesManufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Cordica Medical, Inc.Morristown, TN, United StatesContract manufacturer0000api.fda.gov
Crosstex International, Inc.Sharon, PA, United StatesManufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Excel Medical Products, Inc.Wixom, MI, United StatesContract manufacturer0000api.fda.gov
Great Lakes Dental Technologies, Ltd.Tonawanda, NY, United StatesManufacturer0000api.fda.gov
H & H Co.Hayden, ID, United StatesContract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Hager Worldwide, Inc.Hickory, NC, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Icp, Inc.Green Bay, WI, United StatesSpecification developer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Nucare LLCMontclair, CA, United StatesSpecification developer0000api.fda.gov
Nuflow Products CorporationAustin, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Solmetex, LLCNorthborough, MA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
SWIK Medical SolutionsFarmington Hills, MI, United StatesSpecification developer0000api.fda.gov
Ultralight Optics Inc.Westminster, CA, United StatesSpecification developer0000api.fda.gov
Zirc Dental Products, Inc.Buffalo, MN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Zyris, Inc.Santa Barbara, CA, United StatesSpecification developer0000api.fda.gov

Updated November 3, 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.