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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 30 of 35

Device	Model / Reference	Registries	Class	Status
Fracture and Correction CoLag™ 2	P67 ST872	FDA UDI	Class II	Active
CoLink	P04 N0231	FDA UDI	Class I	Active
CoLink® 2	P43 ST216	FDA UDI	Class II	Unknown
CoLag™	P65 ST840	FDA UDI	Class II	Active
Ibs-B	S67 ST405	FDA UDI	Class II	Active
NeoSpan®	T52 SN020	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™2	P67 ST534	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST850	FDA UDI	Class II	Active
CoLag™	P65 ST900	FDA UDI	Class II	Active
CoLink	P92 ST137	FDA UDI	Class II	Active
In2Bones	P06 S2741	FDA UDI	Class I	Active
Ibs-B	S33 ST726	FDA UDI	Class II	Active
5ms™	P62 ST720	FDA UDI	Class II	Active
Avenger	M07 S002A	FDA UDI	Class I	Active
CoLink Afx	P07 N0031	FDA UDI	Class I	Active
CoLink® 2	P42 ST141	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST726	FDA UDI	Class II	Unknown
Fracture and Correction CoLag™ 2	P67 ST570	FDA UDI	Class II	Active
CoLag 2	P67 ST228	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST227	FDA UDI	Class II	Active
CoLag 2	P68 ST150	FDA UDI	Class II	Active
CoLag™	P65 ST542	FDA UDI	Class II	Active
CoLink® 2	P43 ST224	FDA UDI	Class II	Unknown
Avenger	M70 HC124	FDA UDI	Class II	Active
Ibs-B	S67 ST565	FDA UDI	Class II	Active
CoLink® Sfx	K24 SS109	FDA UDI	Class II	Active
CoLink®	P43 ST122	FDA UDI	Class II	Active
CoLink	V50 ST032	FDA UDI	Class II	Unknown
CoLink™ Afx	P70 ST235	FDA UDI	Class II	Active
Ibs-B	S40 ST832	FDA UDI	Class II	Active
CoLink	P04 N0152	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST230	FDA UDI	Class II	Active
CoLink Mfx	C02 N1501	FDA UDI	Class I	Active
CoLink® 2	P42 ST014	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST003	FDA UDI	Class II	Active
Avenger	M07 N0023	FDA UDI	Class I	Active
Ibs-B	S40 ST828	FDA UDI	Class II	Active
CoLink	P09 N0051	FDA UDI	Class I	Active
CoLink® NeoFuse	V45 ST818	FDA UDI	Class II	Active
Hercules	A40 SP025	FDA UDI	Class II	Active
Hercules®	A80 ST100	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST030	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST045	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST232	FDA UDI	Class II	Active
5ms™	P64 ST408	FDA UDI	Class II	Active
CoLag™	P65 ST328	FDA UDI	Class II	Unknown
CoLink™ Afx	P72 ST130	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST042	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST226	FDA UDI	Class II	Active
CoLag™	P65 ST636	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.