Folio Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Folio Products, Inc. makes
Folio Products, Inc. manufactures medical devices under the SYSTEM 70, SYSTEM 100, SYSTEM 90, SYSTEM 95, and SYSTEM 50 series, designed for specific clinical applications in healthcare settings.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
System 70 And 100 Ref K904246
Regimes: 510(k) Registry: 510(k)System 90 And 95 Ref K905293
Regimes: 510(k) Registry: 510(k)System 50 Ref K905292
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Folio Products, Inc. have in the registry?
The registry currently lists 3 devices for Folio Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Folio Products, Inc.'s devices?
Among its 3 most recently registered devices, Folio Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Folio Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Folio Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Folio Products, Inc. in the registry?
The most recently registered devices listed for Folio Products, Inc. include SYSTEM 70 AND 100, SYSTEM 90 AND 95 and SYSTEM 50.