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., part of Cook GroupLabelled 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 Vance Products with 17 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 1982: VPI-FAIR URETHRAL STENT.
| Mar 1, 1982 | VPI-FAIR URETHRAL STENTK820313 · KOD | 510(k) clearances |
| Mar 1, 1982 | VANCE-JACOBELLIS MICROHEMATURIA CATHETERK812995 · KOD | 510(k) clearances |
| Dec 18, 1981 | VPI URETERAL DILATATION BALLON CATHETERK813278 · EZN | 510(k) clearances |
| Nov 16, 1981 | VANCE-AMBROSE RESECTOSCOPE FORCEPSK812785 · GEN | 510(k) clearances |
| Jul 31, 1981 | VANCE CYSTOSCOPICK812057 · FBK | 510(k) clearances |
| Jul 10, 1981 | VNACE FASCIAL DILATOR SETK811833 · KOE | 510(k) clearances |
| Jun 9, 1981 | VANCE PROSTATIC ASPIRATION SETK811454 · KNW | 510(k) clearances |
| Mar 20, 1981 | POLLACK CHAIN CYSOURETHROGRAM SETK810370 · FGI | 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
