FirmLabelled 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 Ultralite with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 30, 1991: ULTRALITE PANELITE.
| Date | Record | Source |
|---|---|---|
| May 30, 1991 | ULTRALITE PANELITEK910091 · IOB | 510(k) clearances |
| Jun 25, 1986 | ULTRALITE HF1236 HAND AND FOOT SYSTEMK861963 · FTC | 510(k) clearances |
| Mar 31, 1982 | SPECTRA305K820492 · FTC | 510(k) clearances |
| Mar 5, 1982 | SPECTRA (ULTRAVIOLET PRODUCTS)K827123 · | 510(k) clearances |
| Mar 5, 1982 | SPECTRA 305/350K820280 · KGL | 510(k) clearances |
| May 3, 1977 | PSORALITEK761179 · FTC | 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
