Powermedic ApS
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Powermedic ApS is a medical device manufacturer, with 93 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 15 Nov 2026.
- Devices
- 93
Registry facts
- Registries
- FDA GUDID 91
- FDA 510(k) 2
- Device classes
- FDA Class II 93
- Sites and related companies
- Powermedic Aps Denmark
- Identifiers
- DUNS 305378978
Catalogue
Search and filter all 93 devicesShowing 1-50 of 93
Company details
- DUNS number
- 305378978
Sites
- Powermedic Aps DKFEI 3003889343 0 devices
Frequently asked questions
How many devices does Powermedic ApS have in the registry?
The registry currently lists 93 devices for Powermedic ApS. Devices recorded under merged duplicate company entries are counted once.
Which registries list Powermedic ApS's devices?
Among its 50 most recently registered devices, Powermedic ApS has devices listed in FDA GUDID (50 devices).
What risk classes do Powermedic ApS's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Powermedic ApS's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Powermedic ApS in the registry?
The most recently registered devices listed for Powermedic ApS include PowerLaser Basic Vet1200 Cool Grey 30122, PowerLaser Pro 1500 White 45156, PowerLaser Pro1200 Black 45121 and PowerLaser Pro500 Red 45055.