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 15, 2026, FDA's public records list Adven Medical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 21, 2002: REPROCESSED VENODYNE SEQUENTIAL COMPRESSION SLEEVES / WRAP.
| Aug 21, 2002 | REPROCESSED VENODYNE SEQUENTIAL COMPRESSION SLEEVES / WRAPK021528 · JOW | 510(k) clearances |
| Mar 1, 2002 | REPROCESSED DISPOSABLE TROCARSK013987 · KBG | 510(k) clearances |
| Feb 12, 2002 | REPROCESSED USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPSK012675 · JOW | 510(k) clearances |
| Feb 4, 2002 | REPROCESSED USED, DISPOSABLE BLADES, BURS, BITS AND TAPSK012676 · HWE | 510(k) clearances |
| Feb 4, 2002 | REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSK012694 · HWE | 510(k) clearances |
| Jun 28, 1994 | RE-SHARPENABLE SAW BLADESK940501 · GFA | 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
