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Data / Medical devices / Airbrush / United States

FDA-registered makers of Airbrush in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Airbrush (product code KOJ). 5 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.

Device
Airbrush
Product code
KOJ
Country
United States

Makers of Airbrush in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Zest Anchors, LLCCarlsbad, CA, United StatesManufacturer, Repackager or relabeler, Specification developer3January 9, 2004000api.fda.gov
Crystalmark Dental Systems, Inc.Glendale, CA, United StatesManufacturer1December 31, 1996000api.fda.gov
Dentsply LLCYork, PA, United StatesSpecification developer1March 15, 2002000api.fda.gov
Groman Inc.Coconut Creek, FL, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer1April 15, 2003010api.fda.gov
Parkell, Inc.Edgewood, NY, United StatesManufacturer1March 10, 1998000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesContract manufacturer0000api.fda.gov
Danville Materials Research CenterAnaheim, CA, 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.