Is this your brand? Sign in to claim ownership.
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 19 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CoLink® 2 | P43 ST222 | FDA UDI | Class II | Unknown |
| CoLink™ | V35 ST440 | FDA UDI | Class II | Unknown |
| CoLink® | P43 ST026 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST112 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P68 ST234 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST123 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST855 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST445 | FDA UDI | Class II | Active |
| CoLink | P92 ST232 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST260 | FDA UDI | Class II | Active |
| Ibs-B | S67 ST245 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST745 | FDA UDI | Class II | Active |
| In2Bones | C01 N0101 | FDA UDI | Class I | Active |
| 5ms™ | P62 ST714 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST880 | FDA UDI | Class II | Active |
| In2Bones | P04 N0441 | FDA UDI | Class I | Active |
| CoLag™ | P65 ST332 | FDA UDI | Class II | Unknown |
| In2Bones | C01 N1032 | FDA UDI | Class I | Active |
| CoLink® 2 | P42 ST231 | FDA UDI | Class II | Active |
| AlloAid™ | C01-S0002 | FDA UDI | N/A | Active |
| CoLag™ | P65 ST457 | FDA UDI | Class II | Unknown |
| CoLink | P92 ST108 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST211 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST135 | FDA UDI | Class II | Active |
| CoLink® 2 | P42 ST251 | FDA UDI | Class II | Active |
| Ibs-B | S67 ST175 | FDA UDI | Class II | Active |
| CoLink Afx | P07 N0131 | FDA UDI | Class I | Active |
| SubChon | C01 S1205 | FDA UDI | Class I | Active |
| Fracture and Correction CoLag™ 2 | P68 ST240 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST145 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST152 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST257 | FDA UDI | Class II | Active |
| Avenger | M70 SC055 | FDA UDI | Class II | Active |
| CoLink | P04 N0191 | FDA UDI | Class II | Active |
| CoLink™ Afx | P74 ST030 | FDA UDI | Class II | Active |
| In2Bones | C01 N0060 | FDA UDI | Class I | Active |
| CoLink™ Afx | P73 ST224 | FDA UDI | Class II | Active |
| Avenger | M70 SC385 | FDA UDI | Class II | Active |
| CoLink Mini | P90 ST018 | FDA UDI | Class II | Active |
| CoLink™ Afx | P74 ST050 | FDA UDI | Class II | Active |
| CoLag 2 | P68 ST132 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST314 | FDA UDI | Class II | Active |
| CoLink | P92 ST113 | FDA UDI | Class II | Active |
| In2Bones | P08 S0001 | FDA UDI | Class I | Active |
| CoLink™ View | P40 ST231 | FDA UDI | Class II | Active |
| CoLink™ | V35 ST418 | FDA UDI | Class II | Unknown |
| CoLink® NeoFuse | V45 ST860 | FDA UDI | Class II | Unknown |
| CoLink® NeoFuse | P20 ST225 | FDA UDI | Class II | Active |
| CoLink® 2 | P43 ST255 | FDA UDI | Class II | Unknown |
| CoLag 2 | P67 ST438 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
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. |