FDA 510(k) Applications Submitted by Helios Biomedical Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K250420 | 02/13/2025 | Helios Dura Regeneration Matrix | Helios Biomedical Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact