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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 21 of 35

Device	Model / Reference	Registries	Class	Status
CoLink® 2	P42 ST245	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST005	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST716	FDA UDI	Class II	Unknown
CoLink™ Afx	P73 ST220	FDA UDI	Class II	Active
CoLag™	P65 ST228	FDA UDI	Class II	Unknown
5ms™	P62 ST411	FDA UDI	Class II	Active
In2Bones	P07 N0271	FDA UDI	Class I	Active
CoLink®	P43 ST150	FDA UDI	Class II	Active
CoLink	V50 ST018	FDA UDI	Class II	Unknown
CoLink Afx	P07 N1305	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST026	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST028	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST665	FDA UDI	Class II	Unknown
Ibs	C01 S2002	FDA UDI	Class I	Active
CoLag™	P65 ST226	FDA UDI	Class II	Unknown
CoLink	C20 ST171	FDA UDI	Class II	Active
SubChon	C01 S1011	FDA UDI	Class I	Active
Fracture and Correction CoLag™ 2	P67 ST680	FDA UDI	Class II	Active
CoLag 2	P67 ST320	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST845	FDA UDI	Class II	Active
CoLag 2	P67 ST424	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST223	FDA UDI	Class II	Active
CoLag 2	P67 ST212	FDA UDI	Class II	Active
CoLag 2	P67 ST114	FDA UDI	Class II	Active
In2Bones	C01 N0010	FDA UDI	Class I	Active
Rts	M03 S0002	FDA UDI	Class II	Active
CoLink	P04 N0271	FDA UDI	Class I	Active
In2Bones	C01 S0004	FDA UDI	Class I	Active
In2Bones	C01 N0016	FDA UDI	Class I	Active
Hercules	A04 S0147	FDA UDI	Class I	Active
Fracture and Correction CoLag™2	P67 ST538	FDA UDI	Class II	Active
In2Bones	C01 N0062	FDA UDI	Class I	Active
CoLink® NeoFuse	V45 ST832	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™ 2	P67 ST890	FDA UDI	Class II	Active
CoLag™	P65 ST067	FDA UDI	Class II	Active
Fracture and Correction CoLag™2	P67 ST540	FDA UDI	Class II	Active
CoLag 2	P67 ST210	FDA UDI	Class II	Active
CoLag 2	P68 ST157	FDA UDI	Class II	Active
In2Bones	C01 N0071	FDA UDI	Class I	Active
CoLink™ Afx	P72 ST114	FDA UDI	Class II	Active
CoLag™	P65 ST050	FDA UDI	Class II	Active
5ms™	P60 ST647	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST118	FDA UDI	Class II	Active
Ibs-B	S67 ST265	FDA UDI	Class II	Active
CoLink	P04 N0321	FDA UDI	Class I	Active
CoLink®	P40 SP014	FDA UDI	Class II	Active
CoLink	P92 ST220	FDA UDI	Class II	Active
CoLag™	P65 ST426	FDA UDI	Class II	Unknown
CoLink™ Afx	P73 ST026	FDA UDI	Class II	Active
CoLink	P92 ST209	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.