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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 24 of 35

Device	Model / Reference	Registries	Class	Status
Ibs-B	S33 ST840	FDA UDI	Class II	Active
NeoSpan®	T52 SN183	FDA UDI	Class II	Unknown
Rts	M30 SE020	FDA UDI	Class II	Active
5ms™	P62 ST728	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST018	FDA UDI	Class II	Active
CoLink Cfx	P80 ST233	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST850	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™	P65 ST116	FDA UDI	Class II	Unknown
CoLag™	P65 ST680	FDA UDI	Class II	Active
CoLag 2	P67 ST118	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST682	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST210	FDA UDI	Class II	Active
Ibs-B	S33 ST832	FDA UDI	Class II	Active
Ibs-B	S67 ST295	FDA UDI	Class II	Active
In2Bones	P02 N0141	FDA UDI	Class I	Active
CoLag 2	P67 ST340	FDA UDI	Class II	Active
In2Bones	C01 N0121	FDA UDI	Class I	Active
CoLag™	P65 ST314	FDA UDI	Class II	Unknown
Avenger	M07 N0031	FDA UDI	Class I	Active
CoLink®	P43 ST036	FDA UDI	Class II	Active
CoLink® NeoFuse	P20 ST223	FDA UDI	Class II	Active
Hercules	A40 SP145	FDA UDI	Class II	Active
CoLink®	P43 ST038	FDA UDI	Class II	Active
CoLink® NeoFuse	P20 ST125	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST672	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST022	FDA UDI	Class II	Active
CoLag™	P65 ST862	FDA UDI	Class II	Active
CoLag™	P65 ST442	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™ 2	P67 ST645	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST012	FDA UDI	Class II	Active
In2Bones	P08 N0041	FDA UDI	Class I	Active
Hercules	A04 S0135	FDA UDI	Class I	Active
CoLink Cfx	P80 ST221	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST212	FDA UDI	Class II	Active
CoLink Mini	P90 ST012	FDA UDI	Class II	Active
SubChon	C01 S1005	FDA UDI	Class I	Active
CoLink™ Afx	P73 ST238	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST260	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST270	FDA UDI	Class II	Active
CoLag 2	P67 ST140	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST136	FDA UDI	Class II	Active
NeoSpan	T50 SN020	FDA UDI	Class II	Unknown
CoLink Cfx	P80 ST112	FDA UDI	Class II	Active
Ibs-B	S40 ST844	FDA UDI	Class II	Active
CoLink	P92 ST245	FDA UDI	Class II	Active
CoLink® Mfx	C20 ST221	FDA UDI	Class II	Active
CoLink Mfx	C02 N1111	FDA UDI	Class I	Active
Hercules	A04 S0047	FDA UDI	Class I	Active
CoLink® 2	P42 ST261	FDA UDI	Class II	Active
Avenger	M70 HC122	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.