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Sign in to claim this brandIn2Bones, USA
United States·US-MF-000023092
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 7750a, Trinity Road, Cordova, United States
- Website
- www.conmed.com
- —
- —
- [email protected]
- Phone
- +18664266633
- PRRC Contact
- Brent Lalomia
- EUDAMED SRN
- US-MF-000023092
- FDA FEI Number
- 3011580264
- DUNS Number
- —
Catalogue (1746)
Page 8 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CoLink | V50 ST038 | FDA UDI | Class II | Unknown |
| In2Bones | P08 N0071 | FDA UDI | Class I | Active |
| Avenger | M70 SC175 | FDA UDI | Class II | Active |
| CoLink® Mfx | C20 ST121 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P68 ST252 | FDA UDI | Class II | Active |
| In2Bones | P07 N0091 | FDA UDI | Class I | Active |
| CoLink | P04 N0161 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST232 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST655 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST655 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST710 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST334 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST008 | FDA UDI | Class II | Active |
| In2Bones | P06 N0462 | FDA UDI | Class I | Active |
| CoLink™ Afx | P70 ST109 | FDA UDI | Class II | Active |
| Ibs-B | G01 N0121 | FDA UDI | Class I | Active |
| CoLink™ Afx | P73 ST157 | FDA UDI | Class II | Active |
| CoLink | P04 N0201 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST014 | FDA UDI | Class II | Active |
| CoLink | P02 N0231 | FDA UDI | Class I | Active |
| Ibs-B | S67 ST130 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST442 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST754 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST230 | FDA UDI | Class II | Active |
| CoLink® | P43 ST138 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST842 | FDA UDI | Class II | Active |
| NeoSpan | T05 S0001 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST021 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | P20 ST135 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST135 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST722 | FDA UDI | Class II | Active |
| 5ms™ | P62 ST410 | FDA UDI | Class II | Active |
| CoLink NeoFuse | P20 ST201 | FDA UDI | Class II | Active |
| CoLink® | P43 ST047 | FDA UDI | Class II | Active |
| NeoSpan | T50 SN118 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P73 ST212 | FDA UDI | Class II | Active |
| CoLag 2 | P68 ST124 | FDA UDI | Class II | Active |
| CoLink® | P40 SP138 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST424 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST030 | FDA UDI | Class II | Active |
| CoLink | P04 N0142 | FDA UDI | Class II | Active |
| CoLink LapiFix | C01 N4012 | FDA UDI | Class I | Active |
| 5ms™ | P60 ST034 | FDA UDI | Class II | Active |
| Rts | M03 S0003 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST854 | FDA UDI | Class II | Active |
| CoLink™ | V35 ST430 | FDA UDI | Class II | Unknown |
| CoLink® | P43 ST018 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST422 | FDA UDI | Class II | Active |
| CoLink | V50 ST065 | FDA UDI | Class II | Unknown |
| CoLink® | P43 ST126 | FDA UDI | Class II | Active |
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FDA Recalls (2)
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 |
|---|---|---|---|---|
| Aug 18, 2021 | Z-2506-2021 | — | terminated | Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site. |
| Nov 14, 2018 | Z-0670-2019 | — | terminated | The NeoSpan Compression Staple (10x10x10) kits from two lots contain the wrong size drill bit. They contain a 3mm drill bit instead of a 2mm drill bit. |