icotec Instrument, Template for, 3 Segmental Plate 61 mm

GUDID 07640140438634

icotec Instrument, Template for, 3 Segmental Plate 61 mm

icotec AG

Surgical implant template, reusable
Primary Device ID07640140438634
NIH Device Record Key12d4d0ce-b418-473a-9713-c4f4bf5e9e63
Commercial Distribution StatusIn Commercial Distribution
Brand Nameicotec Instrument, Template for, 3 Segmental Plate 61 mm
Version Model Number39-18-3-61
Company DUNS480789465
Company Nameicotec AG
Device Count1
DM Exempttrue
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
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
GS107640140438634 [Primary]

FDA Product Code

KWQAppliance, Fixation, Spinal Intervertebral Body

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

[07640140438634]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-15
Device Publish Date2021-01-07

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.