Is this your brand? Sign in to claim ownership.

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 25 of 35

Device	Model / Reference	Registries	Class	Status
Fracture and Correction CoLag™2	P67 ST532	FDA UDI	Class II	Active
CoLink® 2	P42 ST265	FDA UDI	Class II	Active
CoLink™ Afx	P72 ST032	FDA UDI	Class II	Active
CoLag 2	P67 ST420	FDA UDI	Class II	Active
In2Bones	C01 N2101	FDA UDI	Class I	Active
Ibs-B	S40 ST760	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST110	FDA UDI	Class II	Unknown
Ibs-B	S67 ST290	FDA UDI	Class II	Active
In2Bones	C01 N0082	FDA UDI	Class I	Active
CoLag 2	P67 ST460	FDA UDI	Class II	Active
CoLink Mfx	C02 N1401	FDA UDI	Class I	Active
Ibs-B	S67 ST605	FDA UDI	Class II	Active
Ibs-B	S33 ST748	FDA UDI	Class II	Active
CoLink Mfx	C02 N1201	FDA UDI	Class I	Active
CoLink® 2	P42 ST151	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST687	FDA UDI	Class II	Active
5ms™	P64 ST718	FDA UDI	Class II	Active
Ibs-B	S67 ST275	FDA UDI	Class II	Active
Ibs-B	S33 ST816	FDA UDI	Class II	Active
CoLink® NeoFuse	P02 N0101	FDA UDI	Class I	Active
CoLag™	P65 ST318	FDA UDI	Class II	Unknown
CoLink®	P43 ST028	FDA UDI	Class II	Active
Ibs-B	S33 ST734	FDA UDI	Class II	Active
In2Bones	C01 S1025	FDA UDI	Class I	Active
CoLink® NeoFuse	P20 ST235	FDA UDI	Class II	Active
CoLink® 2	P42 ST016	FDA UDI	Class II	Active
Hercules	A04 S0055	FDA UDI	Class I	Active
Ibs-B	S40 ST848	FDA UDI	Class II	Active
LapiFix	C01 N4101	FDA UDI	Class I	Active
5ms	P06 N1024	FDA UDI	Class II	Active
Ibs-B	S67 ST410	FDA UDI	Class II	Active
Hercules	A04 S0001	FDA UDI	Class II	Active
CoLink® 2	P42 ST165	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST600	FDA UDI	Class II	Unknown
CoLink® 2	P43 ST228	FDA UDI	Class II	Unknown
CoLink™ Afx	P74 ST057	FDA UDI	Class II	Active
Fracture and Correction CoLag™ 2	P67 ST567	FDA UDI	Class II	Active
5ms™	P60 ST470	FDA UDI	Class II	Active
CoLag™	P65 ST216	FDA UDI	Class II	Unknown
CoLink Cfx	P80 ST141	FDA UDI	Class II	Active
CoLink®	P43 ST112	FDA UDI	Class II	Active
CoLink® NeoFuse	V45 ST630	FDA UDI	Class II	Unknown
CoLag™	P65 ST890	FDA UDI	Class II	Active
Fracture and Correction CoLag™	P65 ST111	FDA UDI	Class II	Unknown
Ibs-B	S67 ST235	FDA UDI	Class II	Active
CoLink	P02 N0221	FDA UDI	Class I	Active
CoLink® 2	P42 ST131	FDA UDI	Class II	Active
In2Bones	P08 N0111	FDA UDI	Class I	Active
CoLink® 2	P43 ST214	FDA UDI	Class II	Unknown
CoLink® NeoFuse	V45 ST738	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.