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Data / Medical devices / Cleanser, Denture, Over The Counter / United States

FDA-registered makers of Cleanser, Denture, Over The Counter in the United States: 36 establishments

36 establishments in the United States are registered with the FDA to make Cleanser, Denture, Over The Counter (product code EFT). 1 has 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
Cleanser, Denture, Over The Counter
Product code
EFT
Country
United States

Makers of Cleanser, Denture, Over The Counter in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Diamond Wipes International, Inc.Chino, CA, United StatesContract manufacturer, Repackager or relabeler1May 23, 2008000api.fda.gov
Accupac, LLCMainland, PA, United StatesContract manufacturer0000api.fda.gov
Akervall TechnologiesSaline, MI, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Align Technology, Inc.San Jose, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Andpak, Inc.Morgan Hill, CA, United StatesContract manufacturer0000api.fda.gov
Berrygood Products LLCLake Mary, FL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Cory LabsAlsip, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Dentsply LLCYork, PA, United StatesSpecification developer0000api.fda.gov
Doc Brands, Inc.Knoxville, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Dukal LLCRonkonkoma, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Sarasota, FL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
EverBrands, Inc.Garden Grove, CA, United StatesManufacturer0000api.fda.gov
Gurunanda LLCBuena Park, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Great Lakes Dental Technologies, Ltd.Tonawanda, NY, United StatesSpecification developer0000api.fda.gov
Havpak, Inc.Malvern, PA, United StatesContract manufacturer0000api.fda.gov
Haleon US HOLDINGS LLCWarren, NJ, United StatesSpecification developer0000api.fda.gov
Haleon US Holdings LLCEast Durham, NY, United StatesManufacturer0000api.fda.gov
Haleon US Inc.Lincoln, NE, United StatesManufacturer0000api.fda.gov
Isonic Inc.Chicago, IL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
KP Dental LLCWilmington, DE, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Kulzer, LLCSouth Bend, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Lma Solutions Inc.Raleigh, NC, United StatesSpecification developer0000api.fda.gov
Medtech Products, Inc.Tarrytown, NY, United StatesSpecification developer0000api.fda.gov
Movemints, LLCPittsburgh, PA, United StatesSpecification developer0000api.fda.gov
MicroCare MedicalCommerce City, CO, United StatesManufacturer0000api.fda.gov
New World Imports, Inc.Nashville, TN, United StatesSpecification developer0000api.fda.gov
Orvance, LLCCaledonia, MI, United StatesSpecification developer0000api.fda.gov
Procter & Gamble Co., Regulatory AffairsMason, OH, United StatesSpecification developer0000api.fda.gov
Protech Professional Products, Inc.Boynton Beach, FL, United StatesManufacturer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Redi-2-Paq Home Products, LLCSarasota, FL, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Reprocessor0000api.fda.gov
Regent Labs, Inc.Deerfield Bch, FL, United StatesManufacturer0000api.fda.gov
Sheffield Pharmaceuticals LLCNew London, CT, United StatesContract manufacturer0000api.fda.gov
Thermoplastic Comfort Systems, Inc.Signal Hill, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Tower Laboratories, Ltd.Centerbrook, CT, United StatesManufacturer0000api.fda.gov
Tower Laboratories LtdClinton, CT, United StatesContract manufacturer, 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.