Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Uromed with 10 510(k) clearances. The most recent is a 510(k) clearance dated Apr 20, 2001: MODIFICATION TO CAVERMAP SURGICAL AID.
| Date | Record | Source |
|---|---|---|
| Apr 20, 2001 | MODIFICATION TO CAVERMAP SURGICAL AIDK010213 · ETN | 510(k) clearances |
| Feb 1, 2001 | MODIFICATION TO CAVERMAP SURGICAL AIDK010098 · FGM | 510(k) clearances |
| Apr 21, 2000 | CAVERMAP SURGICAL AIDK000507 · ETN | 510(k) clearances |
| Feb 11, 2000 | CAVERMAP SURGICAL AIDK993436 · FGM | 510(k) clearances |
| May 13, 1999 | UROMED BRACHYTHERAPHY IODINE-125 SOURCESK982226 · KXK | 510(k) clearances |
| May 22, 1998 | UROMED SLING KITK980717 · KNA | 510(k) clearances |
| Mar 31, 1998 | UROMED PATCHK974600 · MNG | 510(k) clearances |
| Jan 30, 1998 | UROMED NEEDLE GRASPERK974137 · OCW | 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
