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Data / Medical devices / Drill, Dental, Intraoral / United States

FDA-registered makers of Drill, Dental, Intraoral in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Drill, Dental, Intraoral (product code DZA). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 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.

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Device
Drill, Dental, Intraoral
Product code
DZA
Country
United States

Makers of Drill, Dental, Intraoral in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Arnold Tuber IndustriesOrchard Park, NY, United StatesManufacturer0000api.fda.gov
Bicon, LLCBoston, MA, United StatesSpecification developer0000api.fda.gov
Brasseler U.S.A. Dental, LLCSavannah, GA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Coltene/Whaledent Inc.Cuyahoga Falls, OH, United StatesManufacturer0000api.fda.gov
Creative Endodontic Technology LLCOrmond Beach, FL, United StatesSpecification developer0000api.fda.gov
Dentsply LLCMilford, DE, United StatesManufacturer0000api.fda.gov
Digital Arches Inc.Fountain Valley, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
DPM Usa Corp.Doral, FL, United StatesManufacturer0000api.fda.gov
Ilumi Sciences IncChantilly, VA, United StatesManufacturer0000api.fda.gov
Keystone Dental Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
LISI MEDICAL RemmeleCoon Rapids, MN, United StatesContract manufacturer0000api.fda.gov
Oco BiomedicalAlbuquerque, NM, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesContract manufacturer0000api.fda.gov
Osseo Scientific, LLCDover Township, NJ, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Power Dental USA, Inc.McHenry, IL, United StatesRemanufacturer, Repackager or relabeler0000api.fda.gov
SKY DENT Corp for dental tradingNew York, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Surgikor, LLCLos Angeles, CA, United StatesSpecification developer0000api.fda.gov
Tulsa Dental Products LLCJohnson City, TN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Veridiam, LLCOceanside, CA, United StatesContract manufacturer0000api.fda.gov
Zuga Medical, Inc.Cleveland, OH, United StatesManufacturer0000api.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.