Christie Medical Holdings, Inc.
United Statesfrom the FDA registration address FDA FEI 3008161930
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Christie Medical Holdings, Inc. makes
Christie Medical Holdings, Inc. manufactures handheld and mobile multi-spectral imaging devices designed for vascular visualization. These include the VeinViewer 4.0 Vision2, VeinViewer 3.0 Flex, and the Presygen/si-1, which enhance the visibility of blood vessels during medical procedures.
The company’s devices are regulated under FDA classifications, including Class I and Class II, with submissions recorded via 510(k) and UDI registries. The portfolio is listed in the US under FDA requirements.
Catalogue
- Registry: GUDID
- Registry: GUDID
Presygen/si-1 Ref K171245
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008161930
- DUNS number
- 117398857
- Address
- 1201 Upsala Road, Sanford, FL, 32771
Frequently asked questions
How many devices does Christie Medical Holdings, Inc. have in the registry?
The registry currently lists 3 devices for Christie Medical Holdings, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Christie Medical Holdings, Inc.'s devices?
Among its 3 most recently registered devices, Christie Medical Holdings, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Christie Medical Holdings, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Christie Medical Holdings, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Christie Medical Holdings, Inc. in the registry?
The most recently registered devices listed for Christie Medical Holdings, Inc. include VeinViewer 4.0 Vision2, VeinViewer 3.0 Flex and Presygen/si-1.