Tutogen Medical U.S., Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Tutogen Medical U.S., Inc. makes
Tutogen Medical U.S., Inc. manufactures the Tutopatch, a medical adhesive patch designed for wound management, and the Tutodent Dental Membrane, a barrier membrane used in dental procedures to promote tissue regeneration.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Tutopatch Ref K991296
510(k) 510(k)Tutodent Dental Membrane Ref K073097
510(k) 510(k)
Frequently asked questions
How many devices does Tutogen Medical U.S., Inc. have in the registry?
The registry currently lists 2 devices for Tutogen Medical U.S., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tutogen Medical U.S., Inc.'s devices?
Among its 2 most recently registered devices, Tutogen Medical U.S., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tutogen Medical U.S., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tutogen Medical U.S., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tutogen Medical U.S., Inc. in the registry?
The most recently registered devices listed for Tutogen Medical U.S., Inc. include TUTOPATCH and TUTODENT DENTAL MEMBRANE.