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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 28 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| CoLag 2 | P67 ST434 | FDA UDI | Class II | Active |
| CoLink® | P43 ST142 | FDA UDI | Class II | Active |
| CoLink® | P43 ST155 | FDA UDI | Class II | Active |
| CoLink® 2 | P43 ST245 | FDA UDI | Class II | Unknown |
| Avenger | M70 SC255 | FDA UDI | Class II | Active |
| CoLink™ Afx | P73 ST160 | FDA UDI | Class II | Active |
| 5ms™ | P60 ST450 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST224 | FDA UDI | Class II | Active |
| CoLink | P04 N0112 | FDA UDI | Class II | Active |
| Avenger | M70 SC065 | FDA UDI | Class II | Active |
| CoLag 2 | P68 ST136 | FDA UDI | Class II | Active |
| Avenger | M70 SC165 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST895 | FDA UDI | Class II | Active |
| CoLink™ Afx | P72 ST137 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST536 | FDA UDI | Class II | Active |
| 5ms™ | P62 ST430 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST824 | FDA UDI | Class II | Active |
| CoLink Mfx | C02 N1114 | FDA UDI | Class I | Active |
| CoLag 2 | P67 ST316 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST233 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST340 | FDA UDI | Class II | Unknown |
| 5ms™ | P62 ST713 | FDA UDI | Class II | Active |
| CoLink Mfx | C02 N1202 | FDA UDI | Class I | Active |
| Ibs-B | S40 ST724 | FDA UDI | Class II | Active |
| CoLink Mfx | C02 N1503 | FDA UDI | Class I | Active |
| Fracture and Correction CoLag™ 2 | P67 ST562 | FDA UDI | Class II | Active |
| CoLink™ | V30 ST234 | FDA UDI | Class II | Unknown |
| Ibs-B | S33 ST830 | FDA UDI | Class II | Active |
| CoLink® 2 | P43 ST240 | FDA UDI | Class II | Unknown |
| Fracture and Correction CoLag™ 2 | P67 ST838 | FDA UDI | Class II | Active |
| CoLink | P70 ST302 | FDA UDI | Class II | Active |
| CoLink | P04 N0141 | FDA UDI | Class II | Active |
| CoLink® NeoFuse | V45 ST816 | FDA UDI | Class II | Unknown |
| Ibs-B | S33 ST752 | FDA UDI | Class II | Active |
| CoLink™ | V35 ST422 | FDA UDI | Class II | Unknown |
| CoLink™ Afx | P73 ST042 | FDA UDI | Class II | Active |
| CoLink® | P07 N0311 | FDA UDI | Class I | Active |
| CoLag™ | P65 ST687 | FDA UDI | Class II | Active |
| Ibs-B | S33 ST760 | FDA UDI | Class II | Active |
| 5ms™ | P64 ST416 | FDA UDI | Class II | Active |
| Avenger | M70 SC285 | FDA UDI | Class II | Active |
| CoLink® 2 | P42 ST155 | FDA UDI | Class II | Active |
| CoLink™ Afx | P70 ST203 | FDA UDI | Class II | Active |
| Rts | M30 SE010 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST455 | FDA UDI | Class II | Unknown |
| CoLag™ | P65 ST540 | FDA UDI | Class II | Active |
| Ibs-B | S40 ST846 | FDA UDI | Class II | Active |
| CoLag™ | P65 ST875 | FDA UDI | Class II | Active |
| In2Bones | P02 N0021 | FDA UDI | Class I | Active |
| CoLink™ Afx | P72 ST118 | 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. |