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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 6 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| In2Bones | P07 N1601 | FDA UDI | Class I | Active |
| In2Bones | P07 N0251 | FDA UDI | Class I | Active |
| CoLink | P04 N0261 | FDA UDI | Class I | Active |
| Hercules | A08 S0001 | FDA UDI | Class I | Active |
| CoLink Mini | P90 ST107 | FDA UDI | Class II | Active |
| In2Bones | P07 N0171 | FDA UDI | Class I | Active |
| CoLink® Sfx | K24 SS216 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST695 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST111 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P68 ST262 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST126 | FDA UDI | Class II | Active |
| CoLink® | P40 SP013 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST014 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST836 | FDA UDI | Class II | Unknown |
| Hercules | A40 SP045 | FDA UDI | Class II | Active |
| 5ms™ | P64 ST422 | FDA UDI | Class II | Active |
| CoLag 2 | P68 ST126 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST250 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ | P65 ST120 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST675 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST567 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST550 | FDA UDI | Class II | Active |
| CoLink | P08 N1205 | FDA UDI | Class I | Active |
| CoLink® NeoFuse | V45 ST822 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST447 | FDA UDI | Class II | Unknown |
| CoLink® | P43 ST060 | FDA UDI | Class II | Active |
| 5ms | P06 N1051 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST847 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™2 | P67 ST555 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST110 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST628 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P70 ST133 | FDA UDI | Class II | Active |
| CoLink® 2 | P04 N0281 | FDA UDI | Class I | Active |
| 5ms™ | P62 ST420 | FDA UDI | Class II | Active |
| In2Bones | P02 N0151 | FDA UDI | Class I | Active |
| CoLag™ | P65 ST865 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST330 | FDA UDI | Class II | Unknown |
| CoLink | P92 ST109 | FDA UDI | Class II | Active |
| CoLink | P08 N1204 | FDA UDI | Class I | Active |
| In2Bones | P07 S0141 | FDA UDI | Class I | Active |
| CoLink™ Afx | P73 ST140 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST247 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST245 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST820 | FDA UDI | Class II | Active |
| CoLink® 2 | P43 ST210 | FDA UDI | Class II | Unknown |
| CoLink | P04 N0301 | FDA UDI | Class I | Active |
| 5ms™ | P62 ST413 | FDA UDI | Class II | Active |
| CoLink Cfx | P08 N1206 | FDA UDI | Class I | Active |
| Ibs-B | G01 N0086 | FDA UDI | Class I | Active |
| CoLink Afx | P07 N1301 | 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. |