First Call, Inc.
Country not established
- Devices
- 2
What First Call, Inc. makes
First Call, Inc. manufactures metallic coronary bypass markers and suturing washers, which are used during coronary artery bypass grafting procedures to enhance surgical precision and visibility of graft placement.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. The company is based in the United States.
Catalogue
- Registry: GUDID
Suturing Washer Ref K052642
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 015526185
Frequently asked questions
How many devices does First Call, Inc. have in the registry?
The registry currently lists 2 devices for First Call, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list First Call, Inc.'s devices?
Among its 2 most recently registered devices, First Call, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do First Call, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for First Call, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from First Call, Inc. in the registry?
The most recently registered devices listed for First Call, Inc. include Coronary Bypass Marker Rev1 and SUTURING WASHER.