Modern Module, Inc.
South KoreaFDA applicant, unverified
- Devices
- 1
What Modern Module, Inc. makes
Modern Module, Inc. manufactures the OMNIVISION, a medical imaging device designed for diagnostic imaging purposes, likely within radiology or endoscopy applications.
The OMNIVISION is classified as a Class II device under FDA regulations and is authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Omnivision Ref K110040
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Modern Module, Inc. have in the registry?
The registry currently lists 1 device for Modern Module, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Modern Module, Inc.'s devices?
Among its 1 most recently registered device, Modern Module, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Modern Module, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Modern Module, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Modern Module, Inc. in the registry?
The most recently registered devices listed for Modern Module, Inc. include OMNIVISION.