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Data / Medical devices / Tester, Pulp / United States

FDA-registered makers of Tester, Pulp in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Tester, Pulp (product code EAT). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Tester, Pulp
Product code
EAT
Country
United States

Makers of Tester, Pulp in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Kerr CorporationOrange, CA, United StatesComplaint file establishment, Specification developer4June 19, 2002000api.fda.gov
Kerr CorporationPomona, CA, United StatesSpecification developer2April 7, 1997000api.fda.gov
Parkell, Inc.Edgewood, NY, United StatesManufacturer1May 9, 1995000api.fda.gov
Coltene/Whaledent Inc.Cuyahoga Falls, OH, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Ecotec ManufacturingOkeechobee, FL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Pac-Dent Inc.Brea, CA, United StatesManufacturer0000api.fda.gov
Stoner IncorporatedQuarryville, PA, United StatesContract manufacturer, 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.