Microcopy, Div. of Neo-Flo, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Microcopy, Div. of Neo-Flo, Inc. makes
Microcopy manufactures the QUICKNIT, a surgical mesh device designed for hernia repair and abdominal wall reconstruction, intended for use in minimally invasive procedures.
The QUICKNIT is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Nova Diamond Ref K885233
Regimes: 510(k) Registry: 510(k)Dry Tips Ref K890734
Regimes: 510(k) Registry: 510(k)Quicknit Ref K131799
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microcopy, Div. of Neo-Flo, Inc. have in the registry?
The registry currently lists 3 devices for Microcopy, Div. of Neo-Flo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microcopy, Div. of Neo-Flo, Inc.'s devices?
Among its 3 most recently registered devices, Microcopy, Div. of Neo-Flo, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Microcopy, Div. of Neo-Flo, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Microcopy, Div. of Neo-Flo, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Microcopy, Div. of Neo-Flo, Inc. in the registry?
The most recently registered devices listed for Microcopy, Div. of Neo-Flo, Inc. include NOVA DIAMOND, DRY TIPS and QUICKNIT.