Seiichi Mfg., Inc.
Country not established
- Devices
- 1
What Seiichi Mfg., Inc. makes
Seiichi Mfg., Inc. manufactures the MAXI-SCOPE and ULTRA-SCOPE, which are optical examination devices designed for medical inspections.
These devices fall under FDA Class I regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Maxi-Scope Or Ultra-Scope Ref K912128
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seiichi Mfg., Inc. have in the registry?
The registry currently lists 1 device for Seiichi Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seiichi Mfg., Inc.'s devices?
Among its 1 most recently registered device, Seiichi Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Seiichi Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Seiichi Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Seiichi Mfg., Inc. in the registry?
The most recently registered devices listed for Seiichi Mfg., Inc. include MAXI-SCOPE OR ULTRA-SCOPE.