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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 10 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CoLag™ | P65 ST445 | FDA UDI | Class II | Unknown |
| Ibs-B | S33 ST740 | FDA UDI | Class II | Active |
| Ibs-B | S67 ST585 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST626 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST830 | FDA UDI | Class II | Active |
| CoLink™ View | P40 SP641 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST755 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P70 ST113 | FDA UDI | Class II | Active |
| CoLink™ View | P40 ST632 | FDA UDI | Class II | Active |
| 5ms™ | P62 ST422 | FDA UDI | Class II | Active |
| CoLink NeoFuse | P20 ST101 | FDA UDI | Class II | Active |
| CoLink | P92 ST132 | FDA UDI | Class II | Active |
| CoLink | P92 ST120 | FDA UDI | Class II | Active |
| CoLink Afx | P07 N0051 | FDA UDI | Class I | Active |
| CoLink® 2 | P42 ST238 | FDA UDI | Class II | Active |
| CoLink | P92 ST128 | FDA UDI | Class II | Active |
| CoLink® 2 | P43 ST238 | FDA UDI | Class II | Unknown |
| CoLink® | P43 ST050 | FDA UDI | Class II | Active |
| CoLink | P92 ST030 | FDA UDI | Class II | Active |
| CoLag 2 | P67 ST436 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST650 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST322 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P73 ST040 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST226 | FDA UDI | Class II | Active |
| Ibs-B | G01 N0071 | FDA UDI | Class I | Active |
| CoLink™ Afx | P73 ST128 | FDA UDI | Class II | Active |
| CoLink | V50 ST026 | FDA UDI | Class II | Unknown |
| Fracture and Correction CoLag™ 2 | P67 ST636 | FDA UDI | Class II | Active |
| 5ms™ | P64 ST708 | FDA UDI | Class II | Active |
| In2Bones | C01 N0001 | FDA UDI | Class I | Active |
| CoLink | P04 N0241 | FDA UDI | Class I | Active |
| Avenger | M70 HC220 | FDA UDI | Class II | Active |
| CoLink | P92 ST016 | FDA UDI | Class II | Active |
| Quantum | M05 00791 | FDA UDI | Class I | Active |
| Ibs-B | S67 ST400 | FDA UDI | Class II | Active |
| CoLink® | P43 ST014 | FDA UDI | Class II | Active |
| Fracture and Correction CoLag™ 2 | P67 ST630 | FDA UDI | Class II | Active |
| CoLink | P70 ST007 | FDA UDI | Class II | Active |
| CoLink Afx | P07 N0141 | FDA UDI | Class I | Active |
| 5ms | P06 N1031 | FDA UDI | Class II | Active |
| CoLink | P04 N0121 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST214 | FDA UDI | Class II | Active |
| Avenger Radial Head | M07 S002B | FDA UDI | Class I | Active |
| 5ms™ | P62 ST722 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST240 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST715 | FDA UDI | Class II | Active |
| In2Bones | P06 N0472 | FDA UDI | Class I | Active |
| CoLink® 2 | P43 ST260 | FDA UDI | Class II | Unknown |
| In2Bones | C01 N0091 | FDA UDI | Class I | Active |
| Fracture and Correction CoLag™ 2 | P67 ST565 | 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. |