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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 4 of 35

Device	Model / Reference	Registries	Class	Status
CoLag 2	P67 ST226	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST060	FDA UDI	Class II	Active
Fracture and Correction CoLag™2	P67 ST542	FDA UDI	Class II	Active
CoLag 2	P67 ST218	FDA UDI	Class II	Active
CoLag 2	P67 ST147	FDA UDI	Class II	Active
5ms™	P64 ST413	FDA UDI	Class II	Active
CoLink	P08 N1102	FDA UDI	Class I	Active
CoLink	P92 ST218	FDA UDI	Class II	Active
CoLink®	P43 ST136	FDA UDI	Class II	Active
Hercules	A02 S0001	FDA UDI	Class I	Active
CoLink™ Afx	P74 ST016	FDA UDI	Class II	Active
CoLink	P92 ST150	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST008	FDA UDI	Class II	Active
Avenger	M70 SC095	FDA UDI	Class II	Active
CoLink Mini	P90 ST013	FDA UDI	Class II	Active
CoLink Mini	P09 N0042	FDA UDI	Class I	Active
Rts	M40 SE010	FDA UDI	Class II	Active
CoLink™ View	P40 ST622	FDA UDI	Class II	Active
CoLag 2	P67 ST336	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST230	FDA UDI	Class II	Active
In2Bones	P04 S0242	FDA UDI	Class I	Active
CoLink™ Afx	P73 ST218	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST662	FDA UDI	Class II	Active
Ibs-B	S67 ST280	FDA UDI	Class II	Active
Ibs-B	S33 ST838	FDA UDI	Class II	Active
Ibs-B	S40 ST740	FDA UDI	Class II	Active
In2Bones	P07 N0121	FDA UDI	Class I	Active
Avenger	M70 SC275	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST670	FDA UDI	Class II	Unknown
5ms™	P60 ST757	FDA UDI	Class II	Active
5ms™	P60 ST557	FDA UDI	Class II	Active
CoLink™ Afx	P74 ST034	FDA UDI	Class II	Active
Ibs-B	S40 ST842	FDA UDI	Class II	Active
CoLag 2	P68 ST130	FDA UDI	Class II	Active
CoLink® 2	P42 ST022	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST034	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST852	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST242	FDA UDI	Class II	Active
CoLag 2	P67 ST440	FDA UDI	Class II	Active
5ms	P06 N1042	FDA UDI	Class II	Active
CoLag™	P65 ST222	FDA UDI	Class II	Unknown
CoLink® NeoFuse	V45 ST730	FDA UDI	Class II	Unknown
Hercules	A04 S0035	FDA UDI	Class I	Active
NeoSpan	T50 SN008	FDA UDI	Class II	Unknown
In2Bones	P09 N0011	FDA UDI	Class I	Active
CoLink™ Afx	P72 ST124	FDA UDI	Class II	Active
Ibs-B	S33 ST846	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST652	FDA UDI	Class II	Active
5ms™	P60 ST657	FDA UDI	Class II	Active
Ibs-B	S67 ST600	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.