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Data / Medical devices / Crown And Bridge, Temporary, Resin / United States

FDA-registered makers of Crown And Bridge, Temporary, Resin in the United States: 39 establishments

39 establishments in the United States are registered with the FDA to make Crown And Bridge, Temporary, Resin (product code EBG). 26 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.

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Device
Crown And Bridge, Temporary, Resin
Product code
EBG
Country
United States

Makers of Crown And Bridge, Temporary, Resin in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
GC America Inc.Alsip, IL, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler7July 9, 2020000api.fda.gov
Dentsply LLCMilford, DE, United StatesContract manufacturer, Manufacturer, Specification developer3September 28, 2010000api.fda.gov
Kerr CorporationOrange, CA, United StatesComplaint file establishment, Manufacturer, Specification developer3February 22, 2002000api.fda.gov
Lang Dental MFG. Co., Inc.Wheeling, IL, United StatesComplaint file establishment, Manufacturer3June 5, 2009010api.fda.gov
Advantage Dental Products, Inc.Clarkston, MI, United StatesManufacturer, Repackager or relabeler2August 4, 2004000api.fda.gov
Danville Materials Research CenterAnaheim, CA, United StatesManufacturer2September 11, 2019000api.fda.gov
Myohealth Technologies, LLCPortland, OR, United StatesManufacturer2November 3, 2020000api.fda.gov
Parkell, Inc.Edgewood, NY, United StatesManufacturer, Repackager or relabeler2May 21, 1999000api.fda.gov
Prismatik Dentalcraft, Inc.Irvine, CA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler2November 3, 2020000api.fda.gov
Pulpdent CorporationWatertown, MA, United StatesManufacturer2June 8, 2012000api.fda.gov
Sterngold Dental LLCAttleboro, MA, United StatesManufacturer2January 24, 2002000api.fda.gov
Zest Anchors, LLCCarlsbad, CA, United StatesRepackager or relabeler, Specification developer2September 11, 2019000api.fda.gov
Dental Plus Usa, LLCSouth Jordan, UT, United StatesRepackager or relabeler, Reprocessor1May 12, 2023000api.fda.gov
Dental Technologies, Inc.Lincolnwood, IL, United StatesManufacturer1February 21, 1996000api.fda.gov
Dentca, Inc.Irvine, CA, United StatesManufacturer1February 5, 2020000api.fda.gov
Formlabs Inc.Somerville, MA, United StatesComplaint file establishment, Specification developer1July 19, 2024000api.fda.gov
Formlabs Ohio, Inc.Millbury, OH, United StatesComplaint file establishment, Manufacturer1July 19, 2024000api.fda.gov
Imagine Milling Technologies, LLCChantilly, VA, United StatesRemanufacturer, Repackager or relabeler1December 12, 2018000api.fda.gov
J. Morita Usa, Inc.Irvine, CA, United StatesRepackager or relabeler, Specification developer1March 4, 2002000api.fda.gov
Keystone IndustriesMyerstown, PA, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler1June 25, 1996000api.fda.gov
Keystone Industries - GibbstownGibbstown, NJ, United StatesManufacturer1June 25, 1996000api.fda.gov
Reliance Orthodontic Products, Inc.Itasca, IL, United StatesContract manufacturer, Specification developer1February 26, 1988000api.fda.gov
Scientific Pharmaceuticals, Inc.Pomona, CA, United StatesContract manufacturer, Manufacturer1August 4, 2004000api.fda.gov
Sprintray Inc.Los Angeles, CA, United StatesManufacturer1November 26, 2024000api.fda.gov
Sprintray Inc.Huntington Beach, CA, United StatesSpecification developer1November 26, 2024000api.fda.gov
Talladium, Inc.Santa Clarita, CA, United StatesManufacturer1April 24, 2015010api.fda.gov
Bicon, LLCBoston, MA, United StatesManufacturer0000api.fda.gov
Contech Medical, Inc.Providence, RI, United StatesContract manufacturer0000api.fda.gov
Dentsply LLCYork, PA, United StatesSpecification developer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Sarasota, FL, United StatesManufacturer, Specification developer0000api.fda.gov
Ivoclar Vivadent Manufacturing, IncSomerset, NJ, United StatesContract manufacturer0000api.fda.gov
Kerr CorporationPomona, CA, United StatesContract manufacturer0000api.fda.gov
Keystone IndustriesCherry Hill, NJ, United StatesManufacturer0000api.fda.gov
Midwest TekNew Albany, IN, United StatesContract manufacturer0000api.fda.gov
Solventum Us LLCEagan, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Solventum US LLCIrvine, CA, United StatesManufacturer0000api.fda.gov
Straumann Manufacturing, Inc.Mansfield, TX, United StatesContract manufacturer0000api.fda.gov
Yates-MotloidElmhurst, IL, United StatesManufacturer0000api.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.