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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 31 of 35

Device	Model / Reference	Registries	Class	Status
Fracture and Correction CoLag™ 2	P67 ST638	FDA UDI	Class II	Active
CoLag™	P65 ST570	FDA UDI	Class II	Active
CoLag™	P65 ST667	FDA UDI	Class II	Active
AlloAid	C01 S1111	FDA UDI	Class I	Active
CoLag 2	P67 ST130	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST116	FDA UDI	Class II	Active
5ms™	P62 ST716	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST667	FDA UDI	Class II	Active
5ms™	P64 ST415	FDA UDI	Class II	Active
BightForce	A40 BFT20	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST634	FDA UDI	Class II	Active
CoLag 2	P68 ST120	FDA UDI	Class II	Active
CoLag™	P65 ST682	FDA UDI	Class II	Active
CoLag™	P65 ST867	FDA UDI	Class II	Active
CoLag™	P65 ST885	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST240	FDA UDI	Class II	Active
CoLink™ View	P40 ST131	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST226	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST208	FDA UDI	Class II	Active
CoLag™	P65 ST420	FDA UDI	Class II	Unknown
CoLag 2	P68 ST138	FDA UDI	Class II	Active
CoLag 2	P67 ST338	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST836	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST047	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST012	FDA UDI	Class II	Active
CoLag™	P65 ST705	FDA UDI	Class II	Active
CoLag™	P65 ST214	FDA UDI	Class II	Unknown
5ms™	P60 ST012	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST020	FDA UDI	Class II	Active
CoLag™	P65 ST632	FDA UDI	Class II	Active
CoLag 2	P67 ST330	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST715	FDA UDI	Class II	Active
CoLag 2	P67 ST137	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST210	FDA UDI	Class II	Unknown
CoLink™ Afx	P73 ST234	FDA UDI	Class II	Active
CoLag 2	P67 ST235	FDA UDI	Class II	Active
CoLink™ Afx	P70 ST016	FDA UDI	Class II	Active
Fracture and Correction CoLag™2	P67 ST550	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST216	FDA UDI	Class II	Active
CoLag™	P65 ST534	FDA UDI	Class II	Active
CoLink™ View	P40 ST642	FDA UDI	Class II	Active
CoLink™ Afx	P73 ST114	FDA UDI	Class II	Active
CoLag 2	P68 ST145	FDA UDI	Class II	Active
5ms™	P62 ST416	FDA UDI	Class II	Active
5ms™	P60 ST760	FDA UDI	Class II	Active
CoLag 2	P67 ST128	FDA UDI	Class II	Active
CoLag 2	P67 ST208	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST045	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST122	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P68 ST236	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.