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 Promex with 18 510(k) clearances. The most recent is a 510(k) clearance dated Dec 19, 2002: BIOPSY SITE TISSUE MARKER DEVICE.
| Date | Record | Source |
|---|---|---|
| Dec 19, 2002 | BIOPSY SITE TISSUE MARKER DEVICEK023450 · NEU | 510(k) clearances |
| Nov 6, 2002 | CO-AXIAL INTRODUCER NEEDLEK022634 · DYB | 510(k) clearances |
| Jul 24, 2001 | VACUUM ASSISTED CORE BIOPSY DEVICEK010400 · KNW | 510(k) clearances |
| Jun 22, 2001 | AUTOMATED CORE BIOPSY DEVICEK011270 · FCG | 510(k) clearances |
| May 1, 2000 | BONE BIOPSY NEEDLEK001132 · KNW | 510(k) clearances |
| Jan 7, 2000 | AUTOMATED CORE BIOPSY DEVICEK994272 · KNW | 510(k) clearances |
| Dec 6, 1999 | MANUAL BONE MARROW BIOPSY DEVICEK993435 · KNW | 510(k) clearances |
| Nov 21, 1997 | PROSTATE SEEDING NEEDLEK973184 · IWJ | 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
