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Data / Medical devices / Scaler, Periodontic / United States

FDA-registered makers of Scaler, Periodontic in the United States: 26 establishments

26 establishments in the United States are registered with the FDA to make Scaler, Periodontic (product code EMN). 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
Scaler, Periodontic
Product code
EMN
Country
United States

Makers of Scaler, Periodontic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alc Enterprises IncBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
American Eagle InstrumentsMissoula, MT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Arnold Tuber IndustriesOrchard Park, NY, United StatesManufacturer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Cislak Manufacturing, Inc.Niles, IL, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Dentalez, Inc., Stardental DivisionLancaster, PA, United StatesManufacturer0000api.fda.gov
GLW, Inc.Englewood Cliffs, NJ, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Goldman Products, Inc.Wauconda, IL, United StatesContract manufacturer, Manufacturer, Remanufacturer0000api.fda.gov
H & H Co.Hayden, ID, United StatesManufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Hu-Friedy MFG. Co. LLCNorthbrook, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
J & J Instruments, LLCNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer0000api.fda.gov
PDT, Inc.Msla, MT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Pilotis Tech LLCBrookhaven, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Premier Dental Products Co.Plymouth Meeting, PA, United StatesSpecification developer0000api.fda.gov
Premier MedicalPhiladelphia, PA, United StatesContract manufacturer0000api.fda.gov
Pro-Dex, Inc.Irvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Pru-Dent MFG., Inc.Schaumburg, IL, United StatesContract manufacturer, Manufacturer, Remanufacturer0000api.fda.gov
Power Dental USA, Inc.McHenry, IL, United StatesContract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler0000api.fda.gov
Pro-Dex IncTustin, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Ranir LLCGrand Rapids, MI, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Sunstar Americas, Inc.Schaumburg, IL, United StatesSpecification developer0000api.fda.gov
Solventum Orthodontics CorporationMonrovia, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Tess Oral Health LLCEau Claire, WI, United StatesSpecification developer0000api.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.