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Data / Medical devices / Dam, Rubber / United States

FDA-registered makers of Dam, Rubber in the United States: 24 establishments

24 establishments in the United States are registered with the FDA to make Dam, Rubber (product code EIE). 8 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
Dam, Rubber
Product code
EIE
Country
United States

Makers of Dam, Rubber in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aseptico, Inc.Woodinville, WA, United StatesComplaint file establishment, Manufacturer1February 3, 1989000api.fda.gov
Coltene/Whaledent Inc.Cuyahoga Falls, OH, United StatesManufacturer, Manufacturer for export, Specification developer1April 16, 1990010api.fda.gov
Den-Mat Holdings, LLCLompoc, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler1December 18, 1985000api.fda.gov
Denali R & D CorporationHanover, MA, United StatesComplaint file establishment, Specification developer1February 18, 2016000api.fda.gov
GC America Inc.Alsip, IL, United StatesManufacturer, Repackager or relabeler1January 25, 2005000api.fda.gov
George Taub Products & Fusion Co., Inc.Jersey City, NJ, United StatesManufacturer1February 18, 2016000api.fda.gov
Prime Dental Manufacturing, Inc.Chicago, IL, United StatesManufacturer1July 19, 2002000api.fda.gov
Pulpdent CorporationWatertown, MA, United StatesManufacturer1September 26, 2002000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Beyond International Inc.Sugar Land, TX, United StatesManufacturer0000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Discus Dental, LLCOntario, CA, United StatesManufacturer0000api.fda.gov
GLO Science, Inc.Garden Grove, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
IPB IncOgden, UT, United StatesContract manufacturer, Manufacturer0000api.fda.gov
J & J Instruments, LLCNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
Mexpo International, Inc.Union City, CA, United StatesContract manufacturer0000api.fda.gov
Philips Oral Healthcare, LLCBothell, WA, United StatesSpecification developer0000api.fda.gov
Smart Denture Conversions, LLCApex, NC, United StatesManufacturer0000api.fda.gov
T33 Dental Inc.Cambridge, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
The Hygenic Company, LLCAkron, OH, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Ultradent Products Inc.South Jordan, UT, United StatesManufacturer0000api.fda.gov
Viarden Lab LLCMission, TX, United StatesManufacturer0000api.fda.gov
Zirc Dental Products, Inc.Buffalo, MN, United StatesComplaint file establishment, 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.