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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
LinkedIn
—
Facebook
—
Phone
+18664266633
PRRC Contact
Brent Lalomia
EUDAMED SRN
US-MF-000023092
FDA FEI Number
3011580264
DUNS Number
—

Catalogue (1746)

Page 7 of 35
DeviceModel / ReferenceRegistriesClassStatus
Avenger M70 SC365
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST690
FDA UDI
Class IIUnknown
CoLag™ P65 ST850
FDA UDI
Class IIActive
Ibs-B S67 ST165
FDA UDI
Class IIActive
Ibs-B S40 ST730
FDA UDI
Class IIActive
CoLag 2 P67 ST455
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST638
FDA UDI
Class IIUnknown
In2Bones P06 N0442
FDA UDI
Class IActive
CoLink™ Afx P70 ST105
FDA UDI
Class IIActive
In2Bones C01 N0014
FDA UDI
Class IActive
Avenger M07 N0021
FDA UDI
Class IActive
CoLink P07 S0002
FDA UDI
Class IActive
In2Bones P04 S0241
FDA UDI
Class IActive
CoLink Mfx C02 N0071
FDA UDI
Class IActive
In2Bones P04 S0231
FDA UDI
Class IActive
CoLink™ Afx P70 ST204
FDA UDI
Class IIActive
CoLink P04 N0104
FDA UDI
Class IIActive
CoLink Cfx P80 ST232
FDA UDI
Class IIActive
In2Bones P02 N0031
FDA UDI
Class IActive
Ibs-B S40 ST860
FDA UDI
Class IIActive
CoLink Afx P42 ST031
FDA UDI
Class IIActive
Fracture and Correction CoLag™ P65 ST208
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ 2 P67 ST880
FDA UDI
Class IIActive
CoLink® Sfx K24 SS254
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST645
FDA UDI
Class IIUnknown
NeoSpan® T05 S0002
FDA UDI
Class IActive
NeoSpan T50 SN010
FDA UDI
Class IIUnknown
CoLink™ Afx P72 ST018
FDA UDI
Class IIActive
CoLink® 2 P42 ST013
FDA UDI
Class IIActive
Ibs-B G01 N0092
FDA UDI
Class IActive
5ms™ P60 ST740
FDA UDI
Class IIActive
SubChon C01 S1209
FDA UDI
Class IActive
CoLag™ P65 ST690
FDA UDI
Class IIActive
In2Bones P07 N0201
FDA UDI
Class IActive
CoLag™ P65 ST855
FDA UDI
Class IIActive
CoLag 2 P68 ST152
FDA UDI
Class IIActive
CoLink™ Afx P70 ST127
FDA UDI
Class IIActive
Avenger M70 HC222
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P68 ST247
FDA UDI
Class IIActive
5ms P06 N0021
FDA UDI
Class IActive
Fracture and Correction CoLag™2 P67 ST545
FDA UDI
Class IIActive
Hercules A02 S0002
FDA UDI
Class IActive
Ibs-B S67 ST170
FDA UDI
Class IIActive
Avenger M70 SC295
FDA UDI
Class IIActive
CoLink® Mfx C20 ST211
FDA UDI
Class IIActive
In2Bones P07 N0291
FDA UDI
Class IActive
CoLag™ P65 ST334
FDA UDI
Class IIUnknown
In2Bones P02 N0051
FDA UDI
Class IActive
CoLink P08 N1201
FDA UDI
Class IActive
CoLink™ Afx P74 ST055
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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.

DateRecall No.ClassStatusReason
Aug 18, 2021Z-2506-2021—terminated

Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.

Nov 14, 2018Z-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.