Prestige Ameritech
United Statesfrom the FDA registration address FDA FEI 3005022483
Prestige Ameritech is a medical device manufacturer, with 869 devices listed in FDA GUDID and FDA 510(k) (FDA Class I and II) as of 13 Nov 2026.
- Devices
- 869
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 863
- FDA 510(k) 6
- Device classes
- FDA Class I 548
- FDA Class II 312
- Identifiers
- FDA FEI 3005022483
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 869 devicesShowing 1-50 of 869
Company details
- FDA FEI number
- 3005022483
- Address
- 7201 Iron Horse Blvd., North Richland Hills, TX, 76180
Frequently asked questions
How many devices does Prestige Ameritech have in the registry?
The registry currently lists 869 devices for Prestige Ameritech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prestige Ameritech's devices?
Among its 50 most recently registered devices, Prestige Ameritech has devices listed in FDA GUDID (50 devices).
What risk classes do Prestige Ameritech's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Prestige Ameritech's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prestige Ameritech in the registry?
The most recently registered devices listed for Prestige Ameritech include PrestigePro 2454, PrestigePro 2451, PrestigePro 2453 and ProGear 7410E3.