Electromed, Inc.
United StatesFDA applicant, unverified FDA FEI 3003007907
Electromed, Inc. is a medical device manufacturer, with 179 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 179
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 173
- FDA 510(k) 6
- Device classes
- FDA Class II 179
- Identifiers
- FDA FEI 3003007907
- DUNS 036514250
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 179 devicesShowing 1-50 of 179
Company details
- FDA FEI number
- 3003007907
- DUNS number
- 036514250
- Address
- 502 SIXTH AVE. N.W., NEW PRAGUE, MN, 56071
Frequently asked questions
How many devices does Electromed, Inc. have in the registry?
The registry currently lists 179 devices for Electromed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electromed, Inc.'s devices?
Among its 50 most recently registered devices, Electromed, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Electromed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Electromed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electromed, Inc. in the registry?
The most recently registered devices listed for Electromed, Inc. include SmartVest, SmartVest SV-32-CL-PP, SmartVest I-VAM-40 and SmartVest SV-28-CM-GK.