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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 2 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CoLink® | P43 ST152 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST042 | FDA UDI | Class II | Unknown |
| 5ms™ | P60 ST755 | FDA UDI | Class II | Active |
| CoLink Afx | P07 N1112 | FDA UDI | Class II | Active |
| Ibs-B | S40 ST758 | FDA UDI | Class II | Active |
| CoLink Cfx | P08 N0031 | FDA UDI | Class I | Active |
| Hercules | A02 S0003 | FDA UDI | Class I | Active |
| Avenger Radial Head | M07 201A00 | FDA UDI | Class I | Active |
| CoLag™ | P65 ST040 | FDA UDI | Class II | Active |
| NeoSpan | T50 SN025 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P74 ST060 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST730 | FDA UDI | Class II | Active |
| Hercules | A20 SP255 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST642 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST016 | FDA UDI | Class II | Active |
| Ibs-B | S40 ST742 | FDA UDI | Class II | Active |
| CoLink® Sfx | K24 SS256 | FDA UDI | Class II | Active |
| In2Bones | P08 N0072 | FDA UDI | Class I | Active |
| 5ms | P06 S0021 | FDA UDI | Class I | Active |
| CoLink™ Afx | P73 ST132 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST452 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST460 | FDA UDI | Class II | Active |
| CoLink Cfx | P80 ST122 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST538 | FDA UDI | Class II | Active |
| Hercules | A20 SP235 | FDA UDI | Class II | Active |
| NeoSpan | T50 SN215 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST887 | FDA UDI | Class II | Active |
| NeoSpan | T50 SN112 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P70 ST205 | FDA UDI | Class II | Active |
| In2Bones | P06 S2322 | FDA UDI | Class I | Active |
| CoLink® 2 | P42 ST255 | FDA UDI | Class II | Active |
| CoLink | C01 N0018 | FDA UDI | Class I | Active |
| CoLink | P92 ST040 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST124 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | P02 N0091 | FDA UDI | Class I | Active |
| CoLink™ | V30 ST236 | FDA UDI | Class II | Unknown |
| 5ms™ | P62 ST428 | FDA UDI | Class II | Active |
| CoLink® | P43 ST116 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST877 | FDA UDI | Class II | Active |
| SubChon | C01 S1507 | FDA UDI | Class I | Active |
| SubChon | C01 S1509 | FDA UDI | Class I | Active |
| CoLink Mfx | C02 S0081 | FDA UDI | Class I | Active |
| CoLink® NeoFuse | V45 ST720 | FDA UDI | Class II | Unknown |
| CoLink® Mfx | C20 ST032 | FDA UDI | Class II | Active |
| CoLink® Mfx | C20 ST031 | FDA UDI | Class II | Active |
| CoLink™ | V35 ST434 | FDA UDI | Class II | Unknown |
| CoLink™ View | P40 ST251 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST126 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST155 | FDA UDI | Class II | Active |
| 5ms™ | P64 ST712 | FDA UDI | Class II | Active |
Related Companies
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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. |