Norco, Inc.
United StatesFDA applicant, unverified FDA FEI 3020756
Norco, Inc. is a medical device manufacturer, with 6 devices listed in FDA 510(k) and FDA GUDID (FDA Class I and II) as of 14 Nov 2026.
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA 510(k) 3
- FDA GUDID 3
- Device classes
- FDA Class I 4
- FDA Class II 2
- Identifiers
- FDA FEI 3020756
- DUNS 043694645
At a glance
Market reach
- United States
- FDA FEI
Catalogue
- Regimes: 510(k) Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Clinical Blood Gas Mixtures Ref K904163
Regimes: 510(k) Registry: 510(k)Lung Diffusion Gas Mixtures Ref K911471
Regimes: 510(k) Registry: 510(k)Carbon Dioxide Flowthrough Laser Mixtures Ref K904162
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3020756
- DUNS number
- 043694645
- Address
- 898 W Gowen Rd, BOISE, ID, 83705
Frequently asked questions
How many devices does Norco, Inc. have in the registry?
The registry currently lists 6 devices for Norco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Norco, Inc.'s devices?
Among its 6 most recently registered devices, Norco, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Norco, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Norco, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Norco, Inc. in the registry?
The most recently registered devices listed for Norco, Inc. include NorLab Medical Blood Gas, NorLab Medical Calibration Gas, NorLab Medical Laser Gas and CLINICAL BLOOD GAS MIXTURES.