I-Tek Medical, Inc.
Country not established FDA establishment FEI 3008627763
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
Company details
- FDA FEI number
- 3008627763
- Address
- 1837 Buerkle Rd, White Bear Lake, MN, 55110
Frequently asked questions
How many devices does I-Tek Medical, Inc. have in the registry?
The registry currently lists 4 devices for I-Tek Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I-Tek Medical, Inc.'s devices?
Among its 4 most recently registered devices, I-Tek Medical, Inc. has devices listed in FDA GUDID (4 devices).
What risk classes do I-Tek Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for I-Tek Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from I-Tek Medical, Inc. in the registry?
The most recently registered devices listed for I-Tek Medical, Inc. include Fiber Optic Illuminator 1136-001, Fiber Optic Illuminator 1102-001, Fiber Optic Illuminator 1090-001 and I-Tek I-150 LED Light Source.