FDA 510(k) Applications Submitted by BIORETEC LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| DEN220030 | 05/04/2022 | RemeOsÖ Screw LAG Solid | Bioretec Ltd. |
| K133950 | 12/23/2013 | ACTIVAPIN HT, FUSE LINK (PRIVATE LABLED FOR FOOTMIND, INC.) | BIORETEC LTD. |
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