Orthocon, Inc.
United StatesFDA applicant, unverified
- Devices
- 40
What Orthocon, Inc. makes
Orthocon, Inc. manufactures resorbable bone pastes, putties, and hemostatic matrices designed for surgical use in orthopedic and cranial procedures. Products include flowable and settable formulations for bone grafting, hemostasis, and burr hole coverage, as well as demineralized bone matrix putties for wound stabilization.
These devices are classified under FDA Class II and Class U, with submissions recorded in the 510(k) registry. The company’s portfolio is regulated under US medical device laws, and all products are listed in the FDA’s 510(k) clearance database.
Catalogue
Search and filter all 40 devicesFrequently asked questions
How many devices does Orthocon, Inc. have in the registry?
The registry currently lists 40 devices for Orthocon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthocon, Inc.'s devices?
Among its 40 most recently registered devices, Orthocon, Inc. has devices listed in FDA 510(k) (40 devices).
What risk classes do Orthocon, Inc.'s devices fall under?
Among its 40 most recently registered devices, the classes recorded for Orthocon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthocon, Inc. in the registry?
The most recently registered devices listed for Orthocon, Inc. include Permatage XT Settable Bone Putty, Permatage Flowable, Permatage XT Settable Nonabsorbable Hemostatic Bone Putty (OS-PER-1001XT) and Montage Flowable Settable, Resorbable Bone Paste.