icotec Instrument T-Handle 38-025

GUDID 07640164841656

icotec Instrument T-Handle

icotec AG

Surgical instrument handle, non-torque-limiting
Primary Device ID07640164841656
NIH Device Record Key5b71af89-02a9-47e4-8bac-c7185517fc49
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument T-Handle
Version Model Number38-025
Catalog Number38-025
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

Device Identifiers

Device Issuing AgencyDevice ID
GS107640164841656 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


[07640164841656]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-08-28
Device Publish Date2018-07-16

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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

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