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Data / Medical devices / Cleaner, Denture, Mechanical / United States

FDA-registered makers of Cleaner, Denture, Mechanical in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Cleaner, Denture, Mechanical (product code JER). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Cleaner, Denture, Mechanical
Product code
JER
Country
United States

Makers of Cleaner, Denture, Mechanical in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Chemlink Laboratories, LLC.Kennesaw, GA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Diversified Chemical Products, IncWilmington, DE, United StatesContract manufacturer0000api.fda.gov
Isonic Inc.Chicago, IL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Medtech Products, Inc.Tarrytown, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Teamwork Packaging, Inc.San Bernardino, CA, United StatesContract manufacturer0000api.fda.gov
Unette CorporationRandolph, NJ, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov

Updated November 2, 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.