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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 15 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| In2Bones | P06 N0751 | FDA UDI | Class I | Active |
| Ibs-B | S40 ST830 | FDA UDI | Class II | Active |
| CoLag 2 | P68 ST140 | FDA UDI | Class II | Active |
| CoLink | P04 N0232 | FDA UDI | Class I | Active |
| Ibs-B | S67 ST240 | FDA UDI | Class II | Active |
| CoLink Mfx | C02 N1112 | FDA UDI | Class I | Active |
| CoLink™ Afx | P72 ST020 | FDA UDI | Class II | Active |
| Ibs-B | S40 ST748 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST560 | FDA UDI | Class II | Active |
| CoLink | P92 ST115 | FDA UDI | Class II | Active |
| CoLink | P04 N0101 | FDA UDI | Class II | Active |
| CoLink™ Afx | P74 ST047 | FDA UDI | Class II | Active |
| NeoSpan® | T52 SN182 | FDA UDI | Class II | Unknown |
| CoLink | P92 ST215 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST555 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST865 | FDA UDI | Class II | Unknown |
| CoLag 2 | P67 ST214 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST834 | FDA UDI | Class II | Active |
| CoLink | C20 ST241 | FDA UDI | Class II | Active |
| CoLink Cfx | P80 ST131 | FDA UDI | Class II | Active |
| In2Bones USA | G05 S1012 | FDA UDI | Class I | Active |
| 5ms™ | P64 ST430 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ | P65 ST128 | FDA UDI | Class II | Unknown |
| CoLink | P92 ST116 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | P02 N0081 | FDA UDI | Class I | Active |
| Ibs-B | S67 ST285 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST436 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST857 | FDA UDI | Class II | Active |
| CoLink™ Afx | P74 ST024 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST104 | FDA UDI | Class II | Active |
| Rts | M30 SE040 | FDA UDI | Class II | Active |
| CoLink | P04 N0105 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST442 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P68 ST257 | FDA UDI | Class II | Active |
| CoLink® | P43 ST030 | FDA UDI | Class II | Active |
| Ibs-B | S40 ST754 | FDA UDI | Class II | Active |
| NeoSpan® | T52 SN018 | FDA UDI | Class II | Unknown |
| CoLag 2 | P67 ST240 | FDA UDI | Class II | Active |
| CoLink™ View | P40 ST634 | FDA UDI | Class II | Active |
| NeoSpan® | T52 SN025 | FDA UDI | Class II | Unknown |
| Ibs-B | S67 ST595 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST765 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P70 ST213 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST832 | FDA UDI | Class II | Active |
| CoLink Cfx | P80 ST222 | FDA UDI | Class II | Active |
| CoLink LapiFix | C01 S4001 | FDA UDI | Class I | Active |
| CoLag™ | P65 ST642 | FDA UDI | Class II | Active |
| CoLink® | P43 ST134 | FDA UDI | Class II | Active |
| CoLink | P92 ST118 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST050 | 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. |