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Data / Medical devices / United States / Doseoptics LLC

Doseoptics LLC: FDA-registered device maker in Lebanon, NH, United States, 2 510(k) clearances

Doseoptics LLC is registered with the FDA (registration 3019552217) in Lebanon, NH, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 29, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3019552217
Address
16 Cavendish Ct, Lebanon, NH, United States, 03766
Owner or operator
DoseOptics LLC (10087183)
Roles
Complaint file establishment, Specification developer
First device listed
January 23, 2023
Registered through
2026
Brand names listed
BeamSite, DoseRT

Devices it lists

DeviceProduct codeClassRoleSource
Accelerator, Linear, MedicalIYE2Complaint file establishment, Specification developeraccessdata.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
March 29, 2024K233622AlignRT PlusIYESubstantially EquivalentVision Rt, Ltd.accessdata.fda.gov
September 15, 2021K212606BeamSiteIYESubstantially EquivalentDoseoptics, LLCaccessdata.fda.gov

Compare with other makers

Updated March 29, 2024. 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.