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 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Devon Medical Products with 12 510(k) clearances. The most recent is a 510(k) clearance dated Mar 19, 2019: Devon 24D Deep Vein Thrombosis (DVT) Prevention Therapy System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 19, 2019 | Devon 24D Deep Vein Thrombosis (DVT) Prevention Therapy SystemK190423 · JOW | 510(k) clearances |
| Feb 21, 2019 | Devon 62 Deep Vein Thrombosis (DVT) Prevention Therapy DeviceK182578 · JOW | 510(k) clearances |
| Dec 18, 2018 | Devon 52 Sequential Compression DeviceK182150 · JOW | 510(k) clearances |
| Feb 6, 2018 | Devon 24R Deep Vein Thrombosis (DVT) Prevention Therapy SystemK173528 · JOW | 510(k) clearances |
| Nov 27, 2017 | Devon 51K172030 · JOW | 510(k) clearances |
| Jul 11, 2017 | Devon 24K170814 · JOW | 510(k) clearances |
| May 31, 2016 | Cirona 6400K161209 · JOW | 510(k) clearances |
| Sep 18, 2015 | Cirona 6300 Disposable Deep Vein Thrombosis (DVT) Prevention SystemK151189 · JOW | 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
