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 15, 2026, FDA's public records list Tillotson Rubber Co., Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 25, 1991: PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES).
| Feb 25, 1991 | PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)K905765 · LYY | 510(k) clearances |
| Sep 5, 1990 | STERILE PATIENT EXAMINATION GLOVESK903756 · LYY | 510(k) clearances |
| Aug 17, 1990 | POWDER FREE, NON-STERILE EXAMINATION GLOVESK903607 · LYY | 510(k) clearances |
| May 7, 1990 | HPI ORTHO SURGEONS' GLOVEK894828 · KGO | 510(k) clearances |
| Feb 21, 1978 | GLOVES, FLOORK780181 · FML | 510(k) clearances |
| Jun 24, 1977 | GLOVES, SURGEONS, LATEXK770704 · 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
