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 15, 2026, FDA's public records list Vee Gee Scientific, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 17, 1995: MODEL 2721 CLINICAL REFRACTOMETER.
| Jan 17, 1995 | MODEL 2721 CLINICAL REFRACTOMETERK941901 · JRE | 510(k) clearances |
| Jan 17, 1995 | MODEL 2740 CLINICAL REFRACTOMETERK941903 · JRE | 510(k) clearances |
| Jan 17, 1995 | MODEL 2730 CLINICAL REFRACTOMETERK941906 · JRE | 510(k) clearances |
| Dec 13, 1994 | MODEL 3471 CLINICAL REFRACTOMETERK941902 · JRE | 510(k) clearances |
| Dec 13, 1994 | MODEL A300CL CLINICAL REFRACTOMETERK941904 · JRE | 510(k) clearances |
| Dec 13, 1994 | MODEL 3461 CLINICAL REFRACTOMETERK941905 · JRE | 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
