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 14, 2026, FDA's public records list Cuda Products Co. with 17 510(k) clearances. The most recent is a 510(k) clearance dated Dec 16, 1998: LIGHTSOURCE OR ILLUMINATOR MODEL I-100.
| Dec 16, 1998 | LIGHTSOURCE OR ILLUMINATOR MODEL I-100K983277 · HBI | 510(k) clearances |
| Aug 18, 1998 | CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCEK981962 · FSS | 510(k) clearances |
| Jul 9, 1998 | CERMAX300 LIGHTSOURCEK981469 · FSS | 510(k) clearances |
| Apr 28, 1998 | VIDEO CAMERA/LIGHTSOURCE COMBINATION UNIT MODEL VCL-150K980350 · GCJ | 510(k) clearances |
| Apr 1, 1998 | LIGHTSOURCE OR ILLUMINATORK980166 · HET | 510(k) clearances |
| Apr 30, 1996 | LIGHTSOURCE OR ILLUMINATORK961074 · FSS | 510(k) clearances |
| May 10, 1995 | INTRAORAL VIDEO SCOPE AND WINDOW TUBEK951019 · EIA | 510(k) clearances |
| Oct 11, 1994 | VIDEO OTOSCOPEK943731 · ERA | 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
