Skip to the page
Get started free

Data / Medical devices / Chair, Dental, Without Operative Unit / United States

FDA-registered makers of Chair, Dental, Without Operative Unit in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Chair, Dental, Without Operative Unit (product code NRU). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in the United StatesWatch these makers
Device
Chair, Dental, Without Operative Unit
Product code
NRU
Country
United States

Makers of Chair, Dental, Without Operative Unit in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A-dec, Inc.Newberg, OR, United StatesManufacturer, Specification developer0000api.fda.gov
Aseptico, Inc.Woodinville, WA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Beaverstate Dental, Inc.Newberg, OR, United StatesManufacturer0000api.fda.gov
Boyd Industries, Inc.Clearwater, FL, United StatesManufacturer0000api.fda.gov
Crosstex International, Inc.Sharon, PA, United StatesManufacturer0000api.fda.gov
Crosstex InternationalRush, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
DCI International, LLCNewberg, OR, United StatesManufacturer0020api.fda.gov
Dentalez Of AlabamaBay Minette, AL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler0000api.fda.gov
Dexta Corp.Napa, CA, United StatesManufacturer0000api.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
Ergonomic Products, Inc.Fall River, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Forest Dental EquipmentBay Minette, AL, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
Mastercraft Dental Co. Of TexasMidlothian, TX, United StatesManufacturer0000api.fda.gov
Medical Technology Industries, Inc.Salt Lake City, UT, United StatesManufacturer0000api.fda.gov
Midmark CorporationVersailles, OH, United StatesManufacturer0000api.fda.gov
Nucare LLCMontclair, CA, United StatesSpecification developer0000api.fda.gov
Palmero Healthcare LLCNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
Petoskey PlasticsPetoskey, MI, United StatesManufacturer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Royal Dental MFG., Inc.Everett, WA, United StatesManufacturer0000api.fda.gov
Summit Dental Systems LLC.Fort Lauderdale, FL, United StatesManufacturer0000api.fda.gov

Updated November 3, 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.