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 13, 2026, FDA's public records list VTS Inc with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 9, 2001: SE-100 VACUUM ERECTION DEVICE.
| Date | Record | Source |
|---|---|---|
| Nov 9, 2001 | SE-100 VACUUM ERECTION DEVICEK012662 · LKY | 510(k) clearances |
| Nov 9, 2001 | SE-300 VACUUM THERAPY SYSTEMK012639 · LKY | 510(k) clearances |
| Nov 9, 2001 | VT-1K012619 · LKY | 510(k) clearances |
| Nov 9, 2001 | SE-200K012620 · LKY | 510(k) clearances |
| Oct 5, 1999 | V.T.S., INC. (V.T.-3)K992442 · LKY | 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
