Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in NetherlandsLabelled 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 Rovers Medical Devices and its 1 subsidiaries with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 2, 2005: CERVEX-BRUSH COMBI.
| Feb 2, 2005 | CERVEX-BRUSH COMBIK043369 · HHT | 510(k) clearances |
| Nov 13, 2000 | ROVERS SPATULAK002520 · HHT | 510(k) clearances |
| May 19, 2000 | ROVERS ENDOCERVEX-BRUSHK001119 · HHT | 510(k) clearances |
| Feb 28, 1995 | CERVEX-BRUSH PAP KITK941472 · HHT | 510(k) clearances |
| Dec 8, 1994 | CERVEX-BRUSH(R), STERILE, SPATULA, CERVICAL, CYTOLOGYK942843 · HHT | 510(k) clearances |
| Jun 27, 1994 | URETHRA-BRUSHK942144 · FDX | 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
