Skip to the page
Get started free

Data / Medical devices / Handpiece, Contra- And Right-Angle Attachment, Dental / United States

FDA-registered makers of Handpiece, Contra- And Right-Angle Attachment, Dental in the United States: 16 establishments

16 establishments in the United States are registered with the FDA to make Handpiece, Contra- And Right-Angle Attachment, Dental (product code EGS). 13 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
Handpiece, Contra- And Right-Angle Attachment, Dental
Product code
EGS
Country
United States

Makers of Handpiece, Contra- And Right-Angle Attachment, Dental in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Angstrom MFG., Inc.Sainte Genevieve, MO, United StatesContract manufacturer, Manufacturer3February 7, 2011000api.fda.gov
Dentalez, Inc., Stardental DivisionLancaster, PA, United StatesManufacturer, Repackager or relabeler, Specification developer3September 19, 2024000api.fda.gov
Dentsply LLCYork, PA, United StatesManufacturer, Specification developer2April 14, 2003000api.fda.gov
Young Dental Manufacturing Co 1, LLC.Earth City, MO, United StatesManufacturer, Repackager or relabeler2June 15, 1979010api.fda.gov
Cordica Medical, Inc.Morristown, TN, United StatesComplaint file establishment, Contract manufacturer1May 16, 1994000api.fda.gov
Crosstex InternationalRush, NY, United StatesRepackager or relabeler, Specification developer1April 14, 2003000api.fda.gov
Essential Dental Systems, Inc.S Hackensack, NJ, United StatesRepackager or relabeler, Specification developer1September 12, 1996000api.fda.gov
Handpiece Headquarters - HPR Inc.Placentia, CA, United StatesSpecification developer1October 23, 2014000api.fda.gov
Lares ResearchChico, CA, United StatesManufacturer, Remanufacturer, Repackager or relabeler1November 7, 2022000api.fda.gov
Pac-Dent Inc.Brea, CA, United StatesRepackager or relabeler, Specification developer1April 14, 2003000api.fda.gov
Preventive Technologies, Inc.Indian Trail, NC, United StatesSpecification developer1February 3, 2000000api.fda.gov
Solventum Us LLCEagan, MN, United StatesComplaint file establishment, Specification developer1May 16, 1994000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Specification developer1May 16, 1994000api.fda.gov
Dentsply LLCMilford, DE, United StatesContract manufacturer0000api.fda.gov
Mti Precision ProductsCoatesville, PA, United StatesManufacturer0000api.fda.gov
Proguard Health Inc.Los Angeles, CA, United StatesContract manufacturer0000api.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.