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Data / Medical devices / Holder, Film, X-Ray / United States

FDA-registered makers of Holder, Film, X-Ray in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Holder, Film, X-Ray (product code EGZ). 0 have a 510(k) clearance or PMA approval on file and 0 have 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
Holder, Film, X-Ray
Product code
EGZ
Country
United States

Makers of Holder, Film, X-Ray in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
BiometerPlus USA, Inc.Fremont, CA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Carwild Corp.New London, CT, United StatesContract manufacturer0000api.fda.gov
Cliktech, LLC.Scottsdale, AZ, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Dentsply LLCYork, PA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Dental Imaging Technologies CorporationQuakertown, PA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Dentsply Sirona Orthodontics Inc.Sarasota, FL, United StatesContract manufacturer0000api.fda.gov
Fredricks/Plasteel Corp.Inkster, MI, United StatesManufacturer0000api.fda.gov
Hager Worldwide, Inc.Hickory, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesManufacturer0000api.fda.gov
Maco Bag Corp.Newark, NY, United StatesContract manufacturer0000api.fda.gov
Microcopy, Division Of Neo-Flo, Inc.Kennesaw, GA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Practicon, Inc.Greenville, NC, United StatesSpecification developer0000api.fda.gov
Proedge Dental ProductsCentennial, CO, United StatesSpecification developer0000api.fda.gov
Ready Set ImportBeverly Hills, CA, United StatesSpecification developer0000api.fda.gov
Steri-Shield IncorporatedFernandina Beach, FL, United StatesManufacturer, Specification developer0000api.fda.gov
Techno-Aide, Inc.Whites Creek, TN, United StatesManufacturer0000api.fda.gov
Temrex Corp.Freeport, NY, United StatesManufacturer0000api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Wolf X-Ray CorpBattleboro, NC, United StatesManufacturer, Repackager or relabeler0000api.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.