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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 18 of 35

Device	Model / Reference	Registries	Class	Status
Fracture and Correction CoLag™2	P67 ST552	FDA UDI	Class II	Active
Hercules	A40 SP035	FDA UDI	Class II	Active
CoLag 2	P67 ST113	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST862	FDA UDI	Class II	Active
CoLink® 2	P42 ST138	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST736	FDA UDI	Class II	Unknown
5ms	P06 N1052	FDA UDI	Class I	Active
Fracture and Correction CoLag™ 2	P67 ST647	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST122	FDA UDI	Class II	Unknown
CoLink Mfx	C02 N0011	FDA UDI	Class I	Active
CoLink™ Afx	P70 ST124	FDA UDI	Class II	Active
CoLag™	P65 ST326	FDA UDI	Class II	Unknown
5ms™	P60 ST542	FDA UDI	Class II	Active
Ibs-B	S33 ST718	FDA UDI	Class II	Active
CoLink® Sfx	K24 SS116	FDA UDI	Class II	Active
Avenger	M07 N0011	FDA UDI	Class I	Active
Rts	M40 SE020	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST004	FDA UDI	Class II	Active
CoLag™	P65 ST695	FDA UDI	Class II	Active
CoLink™	V35 ST426	FDA UDI	Class II	Unknown
In2Bones	P07 N0261	FDA UDI	Class I	Active
In2Bones	P06 S0001	FDA UDI	Class I	Active
CoLag™	P65 ST834	FDA UDI	Class II	Active
CoLag 2	P67 ST450	FDA UDI	Class II	Active
CoLink Mfx	C02 S0091	FDA UDI	Class I	Active
CoLink	P04 N0151	FDA UDI	Class II	Active
Fracture and Correction CoLag™2	P67 ST530	FDA UDI	Class II	Active
CoLink™ View	P40 ST141	FDA UDI	Class II	Active
Avenger	M07 N0025	FDA UDI	Class I	Active
CoLink® 2	P42 ST051	FDA UDI	Class II	Active
BightForce	A40 BFT15	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST050	FDA UDI	Class II	Active
In2Bones	P02 N0041	FDA UDI	Class I	Active
In2Bones	C01 N1021	FDA UDI	Class I	Active
CoLink® 2	P42 ST015	FDA UDI	Class II	Active
CoLink	P92 ST213	FDA UDI	Class II	Active
CoLink Cfx	P80 ST132	FDA UDI	Class II	Active
In2Bones	P08 N0091	FDA UDI	Class I	Active
CoLag™	P65 ST320	FDA UDI	Class II	Unknown
CoLink Cfx	P80 ST121	FDA UDI	Class II	Active
5ms™	P60 ST457	FDA UDI	Class II	Active
CoLink®	P43 ST145	FDA UDI	Class II	Active
Ibs-B	S67 ST315	FDA UDI	Class II	Active
CoLag 2	P67 ST255	FDA UDI	Class II	Active
CoLink	V50 ST022	FDA UDI	Class II	Unknown
CoLink™ Afx	P73 ST010	FDA UDI	Class II	Active
Ibs-B	S67 ST575	FDA UDI	Class II	Active
Fracture and Correction CoLag™2	P67 ST560	FDA UDI	Class II	Active
In2Bones	P09 N0021	FDA UDI	Class I	Active
CoLink® NeoFuse	V45 ST685	FDA UDI	Class II	Unknown

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.