Fujifilm New Development U.S.A., Inc.
Country not established
- Devices
- 8
What Fujifilm New Development U.S.A., Inc. makes
Fujifilm New Development U.S.A., Inc. manufactures surgical imaging and access devices, including a digital video processor with integrated light source for laparoscopic procedures, a trocar for minimally invasive surgery, and a modular surgical system designed for endoscopic applications.
These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
- 510(k) 510(k)
InterLock Trocar Ref K170084
510(k) 510(k)FUJIFILM Surgical System Ref K162836
510(k) 510(k)
Company details
- DUNS number
- 005065629
Frequently asked questions
How many devices does Fujifilm New Development U.S.A., Inc. have in the registry?
The registry currently lists 8 devices for Fujifilm New Development U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fujifilm New Development U.S.A., Inc.'s devices?
Among its 8 most recently registered devices, Fujifilm New Development U.S.A., Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Fujifilm New Development U.S.A., Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Fujifilm New Development U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fujifilm New Development U.S.A., Inc. in the registry?
The most recently registered devices listed for Fujifilm New Development U.S.A., Inc. include Fujifilm Surgical System RC-4440FN, Fujifilm Surgical System EL-580FN, InterLock Trocar Rev A and Fujifilm Surgical System VP-4440FN.