FDA applicant

Dravon Medical, Inc.

Mchenry, IL16 decisions1977–19870 recalls

FDA records 16 decisions for Dravon Medical, Inc. (Mchenry, IL) from 1977 to 1987: 16 510(k) clearances. Most are in product codes KDJ (Set, Administration, For Peritoneal Dialysis…) and FJS (Catheter, Peritoneal, Long-Term Indwelling). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Dravon Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dravon Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dravon Medical, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Dravon Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?