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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 5 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLag™ P65 ST532
FDA UDI
Class IIActive
CoLag™ P65 ST316
FDA UDI
Class IIUnknown
Avenger M70 SC375
FDA UDI
Class IIActive
CoLink® 2 P43 ST252
FDA UDI
Class IIUnknown
In2Bones P06 N0311
FDA UDI
Class IActive
CoLink® P43 ST130
FDA UDI
Class IIActive
CoLink P08 N1302
FDA UDI
Class IActive
5ms™ P60 ST545
FDA UDI
Class IIActive
CoLink P04 N0001
FDA UDI
Class IActive
SubChon M08 N0002
FDA UDI
Class IActive
5ms™ P62 ST408
FDA UDI
Class IIActive
5ms™ P64 ST424
FDA UDI
Class IIActive
CoLink® 2 P43 ST208
FDA UDI
Class IIUnknown
In2Bones C01 S4021
FDA UDI
Class IActive
CoLink P92 ST210
FDA UDI
Class IIActive
CoLink LapiFix C01 N4011
FDA UDI
Class IActive
5ms™ P60 ST652
FDA UDI
Class IIActive
Ibs-B S33 ST834
FDA UDI
Class IIActive
CoLink™ V35 ST420
FDA UDI
Class IIUnknown
In2Bones P02 N0161
FDA UDI
Class IActive
CoLink™ Afx P73 ST222
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST665
FDA UDI
Class IIActive
CoLink C01 S0018
FDA UDI
Class IActive
5ms™ P60 ST540
FDA UDI
Class IIActive
Ibs-B S67 ST300
FDA UDI
Class IIActive
CoLink P92 ST135
FDA UDI
Class IIActive
CoLink V50 ST020
FDA UDI
Class IIUnknown
CoLag™ P65 ST450
FDA UDI
Class IIUnknown
CoLink™ Afx P74 ST032
FDA UDI
Class IIActive
CoLink™ Afx P72 ST010
FDA UDI
Class IIActive
CoLink P92 ST010
FDA UDI
Class IIActive
5ms™ P60 ST570
FDA UDI
Class IIActive
CoLink™ View P40 ST151
FDA UDI
Class IIActive
CoLink® NeoFuse V45 ST675
FDA UDI
Class IIUnknown
Fracture and Correction CoLag™ 2 P68 ST238
FDA UDI
Class IIActive
CoLink P04 N0291
FDA UDI
Class IActive
CoLink P04 N0172
FDA UDI
Class IIActive
CoLink™ Afx P72 ST135
FDA UDI
Class IIActive
CoLink™ Afx P73 ST247
FDA UDI
Class IIActive
CoLag™ P65 ST660
FDA UDI
Class IIActive
Fracture and Correction CoLag™ P65 ST112
FDA UDI
Class IIUnknown
In2Bones P07 N0221
FDA UDI
Class IActive
5ms™ P60 ST790
FDA UDI
Class IIActive
CoLink P08 N1114
FDA UDI
Class IActive
In2Bones C01 N0011
FDA UDI
Class IActive
CoLag 2 P68 ST134
FDA UDI
Class IIActive
CoLink P92 ST112
FDA UDI
Class IIActive
5ms™ P64 ST720
FDA UDI
Class IIActive
5ms™ P64 ST714
FDA UDI
Class IIActive
In2Bones P06 N0761
FDA UDI
Class IActive

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.