Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Radiant Innovation, Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Jun 5, 2024: Non-contact Forehead Thermomete (TH48FE, TH09F, THD2FE).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 5, 2024 | Non-contact Forehead Thermomete (TH48FE, TH09F, THD2FE)K240648 · FLL | 510(k) clearances |
| Dec 6, 2018 | RII Smart IR ThermometerK163601 · FLL | 510(k) clearances |
| Jan 9, 2017 | RII Multi-function Infrared Thermometer, Model TH52ZK162083 · FLL | 510(k) clearances |
| Jul 17, 2012 | NON-CONTACT CLINICAL THERMOMETERK121428 · FLL | 510(k) clearances |
| Dec 6, 2011 | INFRARED EAR THERMOMETERK111637 · FLL | 510(k) clearances |
| Dec 29, 2010 | INFRARED EAR THERMOMETERK103097 · FLL | 510(k) clearances |
| Dec 10, 2010 | RII INFRARED EAR THERMOMETER,K102187 · FLL | 510(k) clearances |
| Jun 29, 2010 | RII INFRARED EAR THERMOMETER, MODEL: TH60NK101253 · FLL | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
