icotec Cervical Cage, Inserter Sleeve, long 41-13-4

GUDID 07640172551400

icotec Cervical Cage, Inserter Sleeve, long

icotec AG

Orthopaedic implant inserter/extractor, reusable
Primary Device ID07640172551400
NIH Device Record Key55dbfb1c-394e-4f26-8974-808174125463
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Cervical Cage, Inserter Sleeve, long
Version Model Number41-13-4
Catalog Number41-13-4
Company DUNS480789465
Company Nameicotec AG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch
Phone+41717570000
Emailinfo@icotec.ch

Device Identifiers

Device Issuing AgencyDevice ID
GS107640172551400 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

[07640172551400]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-05-08
Device Publish Date2021-09-01

Devices Manufactured by icotec AG

07640172553916 - KONG-TL VBR System, Guiding Sleeve for locking screwdriver2026-02-06 KONG-TL VBR System, Guiding Sleeve for locking screwdriver
07640172552544 - CMORE® System, Awl2025-12-02 CMORE® System, Awl
07640172552551 - CMORE® System, Pedicle Probe, Straight2025-12-02 CMORE® System, Pedicle Probe, Straight
07640172552568 - CMORE® System, Drill Guide Sleeve2025-12-02 CMORE® System, Drill Guide Sleeve
07640172552575 - CMORE® System, Drill Guide Stop2025-12-02 CMORE® System, Drill Guide Stop
07640172552582 - CMORE® System, Drill Bit, Ø 2.3 mm2025-12-02 CMORE® System, Drill Bit, Ø 2.3 mm
07640172552599 - CMORE® System, Feeler2025-12-02 CMORE® System, Feeler
07640172552605 - CMORE® System, In-line Handle, AO Coupling2025-12-02 CMORE® System, In-line Handle, AO Coupling
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.