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 Redman, Inc. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Feb 3, 1995: GERONIMO PR.
| Feb 3, 1995 | GERONIMO PRK935751 · ITI | 510(k) clearances |
| Feb 3, 1995 | CHIEF STANDUP WHEELCHAIRK940852 · IPL | 510(k) clearances |
| Feb 3, 1995 | ROAD SAVAGEK940920 · ITI | 510(k) clearances |
| Feb 3, 1995 | CHIEF SRK940919 · IPL | 510(k) clearances |
| Feb 3, 1995 | GERONIMOK935750 · ITI | 510(k) clearances |
| Feb 3, 1995 | RED PACK MANLUAL POWER WHEELCHAIR CONVERSION KITK940851 · ITI | 510(k) clearances |
| Jan 13, 1995 | ROAD WARRIORK935749 · ITI | 510(k) clearances |
| Feb 26, 1987 | REDMAN ACCESSORIESK870298 · KNO | 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
