Printbio, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Printbio, Inc. makes
Printbio, Inc. manufactures 3D-printed surgical mesh products, including the 3DMatrix Surgical Mesh and the 3DMatrix DynaFlex, designed for tissue integration and flexible surgical applications.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) premarket notification process. The company is based in the United States.
Catalogue
3DMatrix DynaFlex (DynaFlex) Ref K243302
Regimes: 510(k) Registry: 510(k)3DMatrix Surgical Mesh Ref K232602
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Printbio, Inc. have in the registry?
The registry currently lists 2 devices for Printbio, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Printbio, Inc.'s devices?
Among its 2 most recently registered devices, Printbio, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Printbio, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Printbio, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Printbio, Inc. in the registry?
The most recently registered devices listed for Printbio, Inc. include 3DMatrix DynaFlex (DynaFlex) and 3DMatrix Surgical Mesh.