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Data / Medical devices / Retainer, Matrix / United States

FDA-registered makers of Retainer, Matrix in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Retainer, Matrix (product code JEP). 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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Get makers of this device in the United StatesWatch these makers
Device
Retainer, Matrix
Product code
JEP
Country
United States

Makers of Retainer, Matrix in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Bioclear Matrix Systems, LLCTacoma, WA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Denovo Dental IncBaldwin Park, CA, United StatesManufacturer0000api.fda.gov
Dockum Research LabIrwindale, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
DSC Dental, LLCSaint George, UT, United StatesManufacturer0000api.fda.gov
Garrison Dental SolutionsSpring Lake, MI, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
GoldenDentRoseville, MI, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Inventex MedicalNiles, IL, United StatesContract manufacturer0000api.fda.gov
Kerr CorporationPomona, CA, United StatesSpecification developer0000api.fda.gov
Nova Biomedical CorporationWaltham, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Nova Biomedical CorporationBillerica, MA, United StatesManufacturer, Remanufacturer0000api.fda.gov
Pilotis Tech LLCBrookhaven, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Practicon, Inc.Greenville, NC, United StatesSpecification developer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Pulpdent CorporationWatertown, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Power Dental USA, Inc.McHenry, IL, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
Ultradent Products Inc.South Jordan, UT, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
White Bite, Inc.Parrish, FL, United StatesSpecification developer0000api.fda.gov
Young Innovations Inc.Algonquin, IL, United StatesSpecification developer0000api.fda.gov
Zirc Dental Products, Inc.Buffalo, MN, United StatesComplaint file establishment, Manufacturer0000api.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.