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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 27 of 35

Device	Model / Reference	Registries	Class	Status
In2Bones	C01 N4021	FDA UDI	Class I	Active
5ms™	P62 ST724	FDA UDI	Class II	Active
CoLag™	P65 ST432	FDA UDI	Class II	Unknown
CoLink	P92 ST226	FDA UDI	Class II	Active
Ibs-B	S40 ST720	FDA UDI	Class II	Active
Avenger	M70 HC018	FDA UDI	Class II	Active
CoLink Mfx	C02 N1113	FDA UDI	Class I	Active
5ms	P06 N1012	FDA UDI	Class II	Active
CoLink®	P43 ST124	FDA UDI	Class II	Active
5ms™	P60 ST032	FDA UDI	Class II	Active
5ms	P06 N1023	FDA UDI	Class II	Active
CoLag 2	P68 ST142	FDA UDI	Class II	Active
5ms	P06 N1011	FDA UDI	Class II	Active
CoLink	P92 ST240	FDA UDI	Class II	Active
CoLink®	P40 SP238	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST140	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST685	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST118	FDA UDI	Class II	Unknown
In2Bones	C01 S0121	FDA UDI	Class I	Active
Fracture and Correction CoLag™ 2	P67 ST640	FDA UDI	Class II	Active
5ms™	P64 ST428	FDA UDI	Class II	Active
CoLink®	P43 ST012	FDA UDI	Class II	Active
CoLink® Sfx	K24 SS214	FDA UDI	Class II	Active
5ms™	P60 ST565	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST010	FDA UDI	Class II	Active
CoLag™	P65 ST547	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST870	FDA UDI	Class II	Active
CoLag™	P65 ST218	FDA UDI	Class II	Unknown
NeoSpan®	T52 SN218	FDA UDI	Class II	Unknown
CoLink™ Afx	P73 ST122	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST867	FDA UDI	Class II	Active
CoLink	P04 N0181	FDA UDI	Class II	Active
CoLink®	P43 ST108	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST826	FDA UDI	Class II	Unknown
Rts	M04 S0001	FDA UDI	Class I	Active
NeoSpan®	T05 S0003	FDA UDI	Class I	Active
CoLink	P04 N0173	FDA UDI	Class II	Active
CoLag 2	P68 ST128	FDA UDI	Class II	Active
CoLink® 2	P43 ST234	FDA UDI	Class II	Unknown
CoLink	P08 N1301	FDA UDI	Class I	Active
CoLink™ Afx	P73 ST216	FDA UDI	Class II	Active
Ibs-B	S40 ST822	FDA UDI	Class II	Active
In2Bones	C01 N0001	FDA UDI	Class I	Active
CoLink™ Afx	P72 ST112	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST120	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST865	FDA UDI	Class II	Active
CoLag 2	P67 ST116	FDA UDI	Class II	Active
CoLink®	P43 ST010	FDA UDI	Class II	Active
5ms	P06 N1032	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST245	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.