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Data / Medical devices / United States / Digital Doc LLC

Digital Doc LLC: FDA-registered device maker in El Dorado Hills, CA, United States, 1 510(k) clearance

Digital Doc LLC is registered with the FDA (registration 3003508094) in El Dorado Hills, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 10, 1998. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003508094
Address
4789 Golden Foothill Pkwy, El Dorado Hills, CA, United States, 95762
Owner or operator
DIGITAL DOC LLC (9048531)
Roles
Manufacturer, Remanufacturer
First device listed
January 23, 2009
Registered through
2026
Brand names listed
GLO X90 Illumination Ring, IRIS 2 Intraoral Camera, IRIS LTE Intraoral Camera, IRIS X80 Intraoral Camera, IRIS X90 Intraoral Camera, LUM X90 Sub-Enamel Illumintion, PXL Intraoral Camera

Devices it lists

DeviceProduct codeClassRoleSource
Unit, Operative DentalEIA1Manufacturer, Remanufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
August 10, 1998K981663DIGITAL DOCEIASubstantially EquivalentDigital Doc, LLCaccessdata.fda.gov

Compare with other makers

Updated August 10, 1998. 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.