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 Tactyl Technologies, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Apr 25, 1996: TACTYLON POWDER FREE EXAMINATION GLOVE.
| Date | Record | Source |
|---|---|---|
| Apr 25, 1996 | TACTYLON POWDER FREE EXAMINATION GLOVEK955464 · LZA | 510(k) clearances |
| Apr 15, 1996 | POWDER FREE TACTYLON SURGEONS GLOVEK955419 · KGO | 510(k) clearances |
| Jan 26, 1996 | LUBRICATED CONDOMK953583 · HIS | 510(k) clearances |
| Apr 13, 1995 | TACTYLON(TM) POWDER FREE SURGEONS GLOVEK950185 · KGO | 510(k) clearances |
| Dec 27, 1994 | TACTYLON(TM) CONDOMK911431 · HIS | 510(k) clearances |
| Nov 21, 1990 | PATIENT EXAMINATION GLOVE/HYPOALLERGENICK905109 · FMC | 510(k) clearances |
| Jul 10, 1990 | TACTYLON TM SURGICAL GLOVEK902831 · KGO | 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
