Heyltex Corp.
Country not established
- Devices
- 1
What Heyltex Corp. makes
Heyltex Corp. manufactures dense hydroxyapatite-based bone grafting materials, designed for use in orthopedic and maxillofacial surgical procedures to promote bone regeneration and integration.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heyltex Corp. have in the registry?
The registry currently lists 1 device for Heyltex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heyltex Corp.'s devices?
Among its 1 most recently registered device, Heyltex Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Heyltex Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Heyltex Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heyltex Corp. in the registry?
The most recently registered devices listed for Heyltex Corp. include ALLOTROPAT/HEYLTEX CORP. BONE GRAFTING DENSE HYDRO.