Anodia Systems
United Statesfrom the FDA registration address FDA FEI 3003917473
Anodia Systems is a medical device manufacturer, with 13 devices listed in FDA GUDID and FDA 510(k) (FDA Class I) as of 13 Nov 2026.
- Devices
- 13
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 9
- FDA 510(k) 4
- Device classes
- FDA Class I 13
- Identifiers
- FDA FEI 3003917473
- DUNS 030080456
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 13 devicesCompany details
- FDA FEI number
- 3003917473
- DUNS number
- 030080456
- Address
- 109 LARRIMORE LANE, Danville, KY, 40422
- Phone
- 8662462548
Frequently asked questions
How many devices does Anodia Systems have in the registry?
The registry currently lists 13 devices for Anodia Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anodia Systems's devices?
Among its 13 most recently registered devices, Anodia Systems has devices listed in FDA 510(k) (4 devices) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Anodia Systems's devices fall under?
Among its 13 most recently registered devices, the classes recorded for Anodia Systems's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Anodia Systems in the registry?
The most recently registered devices listed for Anodia Systems include Zoral Scaler Solution® MAK-Z4, WaterlineX® (01)854542008167(10)204008, PRO-KLEEN 854542008037 and DentaKLEEN® (01)00854542008150(10)3030951384.