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Data / Medical devices / Unit, Operative Dental, Accessories / United States

FDA-registered makers of Unit, Operative Dental, Accessories in the United States: 22 establishments

22 establishments in the United States are registered with the FDA to make Unit, Operative Dental, Accessories (product code NRD). 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
Unit, Operative Dental, Accessories
Product code
NRD
Country
United States

Makers of Unit, Operative Dental, Accessories in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A-dec, Inc.Newberg, OR, United StatesManufacturer0000api.fda.gov
Accs Products, Inc.Lake Zurich, IL, United StatesManufacturer0000api.fda.gov
Adm Tronics Unltd, Inc.Northvale, NJ, United StatesContract manufacturer0000api.fda.gov
Air Techniques, Inc.Melville, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Dentalez Of AlabamaBay Minette, AL, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dntlworks Equipment Corp.Centennial, CO, United StatesManufacturer0000api.fda.gov
Dome IncTarzana, CA, United StatesManufacturer0000api.fda.gov
Dukal LLCRonkonkoma, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Enercon TechnologiesGray, ME, United StatesContract manufacturer0000api.fda.gov
Mastercraft Dental Co. Of TexasMidlothian, TX, United StatesManufacturer0000api.fda.gov
Midmark CorporationVersailles, OH, United StatesManufacturer0000api.fda.gov
Mouthwatch, Inc.Metuchen, NJ, United StatesSpecification developer0000api.fda.gov
Nucare LLCMontclair, CA, United StatesSpecification developer0000api.fda.gov
Perioview, LLCSurprise, AZ, United StatesManufacturer0000api.fda.gov
Practicon, Inc.Greenville, NC, United StatesSpecification developer0000api.fda.gov
Proedge Dental ProductsCentennial, CO, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Sota Cloud CorporationOrange, CA, United StatesManufacturer0000api.fda.gov
Sota Precision Optics, Inc.Orange, CA, United StatesSpecification developer0000api.fda.gov
Stoma Ventures, LLCFort Pierce, FL, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Tech West Inc.Fresno, CA, United StatesManufacturer0000api.fda.gov
Wolf X-Ray CorpBattleboro, NC, 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.