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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 22 of 35
DeviceModel / ReferenceRegistriesClassStatus
CoLink™ Afx P72 ST235
FDA UDI
Class IIActive
SubChon C01 S1211
FDA UDI
Class IActive
CoLink™ Afx P73 ST018
FDA UDI
Class IIActive
In2Bones P06 N0682
FDA UDI
Class IActive
CoLink V50 ST040
FDA UDI
Class IIUnknown
5ms™ P62 ST711
FDA UDI
Class IIActive
CoLag™ P65 ST550
FDA UDI
Class IIActive
CoLink P92 ST216
FDA UDI
Class IIActive
CoLag 2 P68 ST147
FDA UDI
Class IIActive
CoLink P92 ST242
FDA UDI
Class IIActive
CoLag 2 P67 ST237
FDA UDI
Class IIActive
Fracture and Correction CoLag™ 2 P67 ST660
FDA UDI
Class IIActive
CoLink® 2 P43 ST220
FDA UDI
Class IIUnknown
CoLink P92 ST008
FDA UDI
Class IIActive
In2Bones C01 N0013
FDA UDI
Class IActive
Ibs-B S33 ST860
FDA UDI
Class IIActive
In2Bones P07 N0281
FDA UDI
Class IActive
Ibs-B S67 ST260
FDA UDI
Class IIActive
Avenger M70 SC195
FDA UDI
Class IIActive
CoLink G05 S1006
FDA UDI
Class IActive
Fracture and Correction CoLag™ 2 P67 ST830
FDA UDI
Class IIActive
CoLink P04 N0211
FDA UDI
Class IIActive
In2Bones C01 S2168
FDA UDI
Class IActive
CoLink® NeoFuse V45 ST634
FDA UDI
Class IIUnknown
CoLink® 2 P42 ST241
FDA UDI
Class IIActive
Ibs-B S40 ST736
FDA UDI
Class IIActive
CoLink™ Afx P73 ST012
FDA UDI
Class IIActive
NeoSpan® T52 SN185
FDA UDI
Class IIUnknown
Ibs-B S67 ST415
FDA UDI
Class IIActive
CoLag™ P65 ST545
FDA UDI
Class IIActive
CoLink P92 ST147
FDA UDI
Class IIActive
Hercules A40 SP135
FDA UDI
Class IIActive
CoLag 2 P67 ST242
FDA UDI
Class IIActive
CoLag™ P65 ST652
FDA UDI
Class IIActive
CoLink® P43 ST057
FDA UDI
Class IIActive
CoLink P08 N1103
FDA UDI
Class IActive
Hercules A20 SP225
FDA UDI
Class IIActive
CoLink™ View P40 SP611
FDA UDI
Class IIActive
CoLink™ V30 ST240
FDA UDI
Class IIUnknown
In2Bones C01 N1022
FDA UDI
Class IActive
CoLag 2 P67 ST108
FDA UDI
Class IIActive
CoLink® NeoFuse P02 N0071
FDA UDI
Class IActive
CoLag™ P65 ST700
FDA UDI
Class IIActive
CoLink P92 ST111
FDA UDI
Class IIActive
CoLink P92 ST126
FDA UDI
Class IIActive
CoLink Mfx C02 N0031
FDA UDI
Class IActive
CoLink V50 ST055
FDA UDI
Class IIUnknown
CoLink P92 ST028
FDA UDI
Class IIActive
Quantum M05 00801
FDA UDI
Class IActive
Ibs-B S67 ST145
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.