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In2Bones, 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
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +18664266633
PRRC Contact: Brent Lalomia
EUDAMED SRN: US-MF-000023092
FDA FEI Number: 3011580264
DUNS Number: —

Catalogue (1746)

Page 14 of 35

Device	Model / Reference	Registries	Class	Status
CoLink	P92 ST237	FDA UDI	Class II	Active
CoLag 2	P67 ST445	FDA UDI	Class II	Active
CoLink	P92 ST042	FDA UDI	Class II	Active
CoLag 2	P68 ST122	FDA UDI	Class II	Active
CoLink	P92 ST247	FDA UDI	Class II	Active
CoLink	P08 N1111	FDA UDI	Class I	Active
Fracture and Correction CoLag™ 2	P67 ST900	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST022	FDA UDI	Class II	Active
CoLink	C20 ST251	FDA UDI	Class II	Active
5ms	P06 N0061	FDA UDI	Class I	Active
CoLink® NeoFuse	P02 N0011	FDA UDI	Class I	Active
5ms™	P60 ST022	FDA UDI	Class II	Active
Ibs-B	S67 ST590	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST014	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST126	FDA UDI	Class II	Unknown
CoLag™	P65 ST212	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™ 2	P67 ST840	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST220	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST020	FDA UDI	Class II	Active
CoLink® 2	P42 ST161	FDA UDI	Class II	Active
Ibs-B	S67 ST610	FDA UDI	Class II	Active
CoLink	C20 ST271	FDA UDI	Class II	Active
CoLink® Mfx	C20 ST131	FDA UDI	Class II	Active
CoLink	P04 N0311	FDA UDI	Class I	Active
CoLink® NeoFuse	V45 ST655	FDA UDI	Class II	Unknown
CoLink®	P40 SP016	FDA UDI	Class II	Active
CoLink®	P43 ST140	FDA UDI	Class II	Active
CoLink	P92 ST124	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST125	FDA UDI	Class II	Active
CoLag™	P65 ST562	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST207	FDA UDI	Class II	Active
Rts	M03 S0001	FDA UDI	Class II	Active
CoLink™ View	P40 ST612	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST252	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST677	FDA UDI	Class II	Active
In2Bones	C01 N2102	FDA UDI	Class I	Active
CoLag 2	P67 ST432	FDA UDI	Class II	Active
CoLink Mini	P90 ST023	FDA UDI	Class II	Active
CoLink Afx	P07 N1107	FDA UDI	Class II	Active
CoLink Afx	P07 N0101	FDA UDI	Class I	Active
Ibs-B	S67 ST155	FDA UDI	Class II	Active
CoLink Cfx	P80 ST133	FDA UDI	Class II	Active
Avenger	M70 HC118	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST842	FDA UDI	Class II	Active
NeoSpan	T50 SN015	FDA UDI	Class II	Unknown
CoLink Mfx	C02 N0081	FDA UDI	Class I	Active
Avenger	M70 SC085	FDA UDI	Class II	Active
CoLink® 2	P43 ST250	FDA UDI	Class II	Unknown
NeoSpan	T50 SN115	FDA UDI	Class II	Unknown
CoLag™	P65 ST657	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

Conmed Europe BV BE

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.