| OSSIOfiber® Compression Screw | OF1024046S | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation Implant | OF10032210 | FDA UDI | Class II | Active |
| OSSIO® Drill Pack | THN00484 | FDA UDI | Class I | Active |
| OSSIOfiber® Compression Staple | OF1060910S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1024028S | FDA UDI | Class II | Active |
| OSSIOfiber® Threaded Trimmable Fixation Nail | OF1084570 | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation Implant | OF10025160 | FDA UDI | Class II | Active |
| OSSIOfiber® Suture Anchor | OF1034752S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1024026S | FDA UDI | Class II | Active |
| OSSIOfiber® Trimmable Fixation Nail System, Cannulated | OF2054070S | FDA UDI | Class I | Active |
| OSSIOfiber® Compression Screw | OF1073520S | FDA UDI | Class II | Active |
| OSSIOfiber® Trimmable Fixation Nail, Cannulated | OF1054100S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1073512S | FDA UDI | Class II | Active |
| OSSIOfiber® Threaded Trimmable Fixation Nail System | OF2084510 | FDA UDI | Class I | Active |
| OSSIOfiber® Compression Screw | OF1024032S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Staple System | OF2062020S | FDA UDI | Class I | Active |
| OSSIOfiber® Trimmable Fixation Nail System, Cannulated | OF2054100S | FDA UDI | Class I | Active |
| OSSIOfiber® Hammertoe Fixation System | OF20029190 | FDA UDI | Class II | Active |
| OSSIOfiber® Suture Anchor | OF1034755S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1024034S | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation Implant | OF10025161 | FDA UDI | Class II | Active |
| OSSIO® Drill Bit 2.5 mm For Staple | THN00323SP | FDA UDI | Class I | Active |
| OSSIOfiber® Hammertoe Fixation Implant | OF10032211 | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1073526S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Staple | OF1062522S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Staple | OF1062020S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1024044S | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation System | OF20025161 | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1073530S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Staple System | OF2061110S | FDA UDI | Class I | Active |
| OSSIO® Punch Pack | THN00241 | FDA UDI | Class I | Active |
| OSSIOfiber® Compression Screw | OF1073532S | FDA UDI | Class II | Active |
| OSSIOfiber® Suture Anchor | OF1034751S | FDA UDI | Class II | Active |
| OSSIOfiber® Compression Screw | OF1024050S | FDA UDI | Class II | Active |
| OSSIO® Staple Sizing Guide | THN00292 | FDA UDI | Class I | Active |
| OSSIOfiber® Compression Screw | OF1073514S | FDA UDI | Class II | Active |
| OSSIOfiber™ Hammertoe Fixation Implant | 2.9X19 mm straight | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation System | OF20025160 | FDA UDI | Class II | Active |
| OSSIOfiber® Hammertoe Fixation System | OF20032211 | FDA UDI | Class II | Active |
| OSSIO® Tap Pack | THN00239 | FDA UDI | Class I | Active |
| OSSIOfiber® Threaded Trimmable Fixation Nail | K254077 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Suture Anchor 2.5-3.5 mm | K243760 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Compression Staple | K233302 | FDA 510(k) | Class II | Active |
| OSSIOfiber™ Compression Screws | K193660 | FDA 510(k) | Class II | Active |
| OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation Implant | K190652 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Suture Anchor | K254055 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable Fixation Nail | K231272 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Cannulated Trimmable Fixation Nail | K230750 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Compression Staple | K241932 | FDA 510(k) | Class II | Active |
| OSSIOfiber® Suture Anchor | K251309 | FDA 510(k) | Class II | Active |