Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 13, 2026, FDA's public records list LKC Technologies, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated May 19, 2015: RETeval Visual Electrodiagnostic Device.
| Date | Record | Source |
|---|---|---|
| May 19, 2015 | RETeval Visual Electrodiagnostic DeviceK142567 · GWE | 510(k) clearances |
| Oct 25, 1991 | SCOPTOPIC SENSITIVITY TEST-1[SST-1]K914163 · HLX | 510(k) clearances |
| Oct 23, 1991 | ANOMALOSCOPE QUADRANT TEST-6K913962 · HIW | 510(k) clearances |
| Feb 5, 1988 | ANOMALOSCOPE PLATE TEST - 5 [APT-5]K875026 · HIT | 510(k) clearances |
| Jan 12, 1988 | PATTERN DISCRIMINATION PERIMETERK874336 · HPT | 510(k) clearances |
| Mar 4, 1982 | UNIVERSAL TESTING & ANALYSIS SYSTEMSK820414 · GWF | 510(k) clearances |
| Mar 16, 1979 | TELEMETRY, BIOMEDICALK790109 · DRG | 510(k) clearances |
| Aug 4, 1976 | ELECTRORETINOGRAPHK760199 · HLZ | 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
