Stock: ELMD. Includes companies and brands it has bought. Official US government data, updated September 2026.
510(k) clearances
30
De Novo: 0
PMA approvals
0
0 supplements
Recalled products
-
- class I
Adverse event reports
15
- deaths reported
Electromed has - recalled medical device products in - recall actions in the records, - of them class I (the most serious kind).
30 510(k) clearances, 0 De Novo grants and 0 original PMA approvals for high-risk devices, plus 0 PMA supplements (changes to approved devices). The newest decision was on Nov 18, 2022.
15 reports in total: - deaths, 13 injuries and 2 malfunctions were reported. 5 reports were received in 2025. A report alone does not show that the device caused the problem.
Last 15 years
| Year | 510(k) clearance | De Novo grant | PMA approval | PMA supplement |
|---|---|---|---|---|
| 2022 | 1 | 0 | 0 | 0 |
| 2013 | 1 | 0 | 0 | 0 |
Recalled products, class I, and reports received
By product code, all years
All device makers and procedures · ELMD stock page
Official US government data on medical device marketing decisions, recalls (one row per recalled product) and adverse event reports. Company names in the records are linked to ELMD with a reviewed list that includes the companies it has bought. Adverse event reports come from makers, hospitals, doctors and patients; a report alone does not prove that a device caused the problem.
| Year | Recalls | Class I | Reports | Deaths |
|---|
| 2026 | 0 | 0 | 4 | - |
| 2025 | 0 | 0 | 5 | - |
| 2024 | 0 | 0 | 3 | - |
| 2023 | 0 | 0 | 1 | - |