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Sign in to claim this brandMusculoskeletal Transplant Foundation
US
Last updated May 23, 2026
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- US
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Catalogue (72)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dbx® | 048015 | FDA UDI | Class II | Unknown |
| Dbx® | 038025 | FDA UDI | Class II | Active |
| Dbx® | 068025 | FDA UDI | Class II | Active |
| Dbx® | 038010 | FDA UDI | Class II | Active |
| Dbx® | 428025 | FDA UDI | Class II | Active |
| Dbx® | 038100 | FDA UDI | Class II | Active |
| Legacy DBM | 420800 | FDA UDI | Class II | Active |
| Dbx® | 030010 | FDA UDI | Class II | Active |
| Dbx® | 038005 | FDA UDI | Class II | Active |
| Dbx® | 038050 | FDA UDI | Class II | Active |
| Dbx® | 428010 | FDA UDI | Class II | Active |
| Dbx® | 428005 | FDA UDI | Class II | Active |
| Cascade | 910046 | FDA UDI | Class I | Unknown |
| Dbx® | 068050 | FDA UDI | Class II | Active |
| Dbx® | 227010 | FDA UDI | Class II | Active |
| Legacy DBM | 420810 | FDA UDI | Class II | Active |
| Dbx | 227007 | FDA UDI | Class II | Active |
| Dbx® | 227060 | FDA UDI | Class II | Active |
| Dbx® | 048150 | FDA UDI | Class II | Unknown |
| Dbx® | 030025 | FDA UDI | Class II | Active |
| LipoGrafter | 913000 | FDA UDI | Class I | Active |
| Dbx® | 028010 | FDA UDI | Class II | Active |
| Dbx® | 058200 | FDA UDI | Class II | Active |
| QuickGraft | 430PST | FDA UDI | Class II | Active |
| Dbx® | 227055 | FDA UDI | Class II | Active |
| Cascade | 910048 | FDA UDI | Class I | Unknown |
| Dbx® | 048050 | FDA UDI | Class II | Unknown |
| Dbx® | 058025 | FDA UDI | Class II | Active |
| Cascade | 910050 | FDA UDI | Class I | Unknown |
| Dbx® | 028005 | FDA UDI | Class II | Active |
| Legacy DBM | 420802 | FDA UDI | Class II | Active |
| Legacy DBM | 420805 | FDA UDI | Class II | Active |
| Dbx® | 228025 | FDA UDI | Class II | Active |
| Dbx® | 228005 | FDA UDI | Class II | Active |
| Cascade | 910047 | FDA UDI | Class I | Unknown |
| Dbx® | 028100 | FDA UDI | Class II | Active |
| Dbx® | 068100 | FDA UDI | Class II | Active |
| Dbx® | 048010 | FDA UDI | Class II | Unknown |
| Dbx® | 028050 | FDA UDI | Class II | Active |
| Dbx® | 058100 | FDA UDI | Class II | Active |
| Dbx® | 030005 | FDA UDI | Class II | Active |
| Cascade | 910044 | FDA UDI | Class I | Unknown |
| Dbx® | 048025 | FDA UDI | Class II | Unknown |
| Dbx® | 228010 | FDA UDI | Class II | Active |
| Dbx® | 058050 | FDA UDI | Class II | Active |
| Dbx® | 048125 | FDA UDI | Class II | Unknown |
| Dbx® | 227005 | FDA UDI | Class II | Active |
| Legacy DBM | 420801 | FDA UDI | Class II | Active |
| Aft | K042125 | FDA 510(k) | Class II | Active |
| Dbx Demineralized Bone Matrix Putty | K103784 | FDA 510(k) | Class II | Active |
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FDA Recalls (9)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 22, 2023 | Z-1066-2024 | — | open, classified | Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. |
| Dec 22, 2023 | Z-1067-2024 | — | open, classified | Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. |
| Sep 22, 2023 | Z-0323-2024 | — | open, classified | Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery. |
| Mar 29, 2021 | Z-1562-2021 | — | terminated | 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery |
| Aug 15, 2019 | Z-2548-2019 | — | terminated | Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure. |
| Apr 21, 2016 | Z-2004-2016 | — | terminated | AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the sterile field. |
| May 27, 2015 | Z-2210-2015 | — | terminated | Musculoskeletal Transplant Foundation (MTF) is recalling one lot of MTF's Allograft Cortical Pins because the lot was labeled as a 2.0 mm diameter pin and it may contain a 2.4 mm diameter pin. |
| May 27, 2015 | Z-2075-2015 | — | terminated | Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm diameter drill. |
| Dec 4, 2014 | Z-1455-2015 | — | terminated | The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for lot identified above may not be fully intact. |