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Data / Medical devices / Handpiece, Air-Powered, Dental / United States

FDA-registered makers of Handpiece, Air-Powered, Dental in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Handpiece, Air-Powered, Dental (product code EFB). 17 have a 510(k) clearance or PMA approval on file and 1 has 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.

Get makers of this device in the United StatesWatch these makers
Device
Handpiece, Air-Powered, Dental
Product code
EFB
Country
United States

Makers of Handpiece, Air-Powered, Dental in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Young Dental Manufacturing Co 1, LLC.Earth City, MO, United StatesManufacturer, Repackager or relabeler8October 24, 2014000api.fda.gov
Dentalez, Inc., Stardental DivisionLancaster, PA, United StatesManufacturer, Repackager or relabeler7January 6, 2020000api.fda.gov
Electro Medical Systems, L.L.C.Southlake, TX, United StatesRemanufacturer, Repackager or relabeler7December 18, 2017000api.fda.gov
Osseo Scientific, LLCDover Township, NJ, United StatesRepackager or relabeler, Specification developer5March 20, 2008000api.fda.gov
Lares ResearchChico, CA, United StatesManufacturer, Remanufacturer, Repackager or relabeler4September 3, 2021000api.fda.gov
Mti Precision ProductsCoatesville, PA, United StatesManufacturer, Repackager or relabeler4March 20, 2008010api.fda.gov
Handpiece Headquarters - HPR Inc.Placentia, CA, United StatesManufacturer, Specification developer3February 17, 2015000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesManufacturer3September 10, 1997000api.fda.gov
Anodia SystemsDanville, KY, United StatesManufacturer, Repackager or relabeler2July 22, 1993000api.fda.gov
FilmtechBrooklyn, NY, United StatesManufacturer1October 24, 1996000api.fda.gov
Integrated Solutions, Inc.Augusta, GA, United StatesManufacturer1January 31, 1994000api.fda.gov
Kerr CorporationPomona, CA, United StatesComplaint file establishment, Manufacturer1February 21, 1996000api.fda.gov
MicrotechSanta Ana, CA, United StatesManufacturer1October 22, 2002000api.fda.gov
OsteomedAddison, TX, United StatesManufacturer1June 10, 1991000api.fda.gov
Petoskey PlasticsPetoskey, MI, United StatesManufacturer1February 21, 1996000api.fda.gov
Preventive Technologies, Inc.Indian Trail, NC, United StatesSpecification developer1November 15, 1978000api.fda.gov
Tulsa Dental Products LLCJohnson City, TN, United StatesManufacturer, Repackager or relabeler1December 10, 1998000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesContract manufacturer0000api.fda.gov
Proguard Health Inc.Los Angeles, CA, United StatesContract 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.