Infinity KTS224

GUDID 30845854902268

Infinity 2.4mm Guide Sleeve Angled

Conmed Corporation

Surgical drill guide, reusable
Primary Device ID30845854902268
NIH Device Record Key0a672500-b49b-46d4-a2a5-da965bc50750
Commercial Distribution StatusIn Commercial Distribution
Brand NameInfinity
Version Model NumberKTS224
Catalog NumberKTS224
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY
Special Storage Condition, SpecifyBetween 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854648841 [Direct Marking]
GS130845854902268 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

[30845854902268]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-04-06
Device Publish Date2019-10-25

On-Brand Devices [Infinity]

30845854902329Infinity Anteromedial Guide Right 9/10mm
30845854902312Infinity Anteromedial Guide Right 7/8mm
30845854902305Infinity Anteromedial Guide Left 9/10mm
30845854902299Infinity Anteromedial Guide Left 7/8mm
30845854902282Infinity Guide Body
30845854902275Infinity 3.5mm All-Inside Guide Sleeve
30845854902268Infinity 2.4mm Guide Sleeve Angled
30845854902251Infinity 2.4mm Guide Sleeve Straight
30845854902244Infinity PCL Tibial Guide
30845854902237Infinity ACL Tibial Tip Guide
30845854902220Infinity ACL Tibial Elbow Guide
30845854902213Infinity ACL Tibial Footprint Guide
30845854902206Infinity ACL/PCL Femoral Footprint Guide
30845854902190Infinity 3.5mm Tunnel Dilator
30845854901674KPS Infinity Insert Tray
30845854902060Infinity Suture Shuttle
20845854902049Infinity Retro-Reamer 12mm
20845854902032Infinity Retro-Reamer 11mm
20845854902025Infinity Retro-Reamer 10mm
20845854902018Infinity Retro-Reamer 9.5mm
20845854902001Infinity Retro-Reamer 9mm
20845854901998Infinity Retro-Reamer 8.5mm
20845854901981Infinity Retro-Reamer 8mm
20845854901974Infinity Retro-Reamer 7.5mm
20845854901967Infinity Retro-Reamer 7mm
20845854901950Infinity Retro-Reamer 6.5mm
20845854901943Infinity Retro-Reamer 6mm
30845854901810Infinity™ 3.5mm Spade Tip Guide Pin
30845854648814Infinity PCL Tibial Guide
30845854648784Infinity Guide Body
30845854648777Infinity ACL/PCL Femoral Footprint Guide
30845854648760Infinity Anteromedial Guide Right 9/10mm
20845854901806Infinity™ Adjustable Free Loop
20845854901790Infinity™ Femoral Adjustable Loop Button
10845854901786Infinity™ Adjustable Loop Button Cradle
10845854901779Infinity™ Large Tibial Button
10845854901762Infinity™ Standard Tibial Button
20845854648978Infinity™ 3.5mm Spade Tip Guide Pin
20845854649111Infinity™ Large Tibial Button
20845854649104Infinity™ Standard Tibial Button
20845854649074Infinity™ Adjustable Loop Button Cradle
20845854649067Infinity™ Femoral Adjustable Loop Button
30845854083639Infinity 3.5mm Tunnel Dilator
30845854083578Infinity Suture Shuttle
20845854083564Infinity Retro-Reamer 12mm
20845854083557Infinity Retro-Reamer 11mm
20845854083540Infinity Retro-Reamer 10mm
20845854083472Infinity Retro-Reamer 6.5mm
20845854083465Infinity Retro-Reamer 6mm
10845854648841Infinity 2.4mm Guide Sleeve Angled

Trademark Results [Infinity]

Mark Image

Registration | Serial
Company
Trademark
Application Date
INFINITY
INFINITY
98761246 not registered Live/Pending
Zevex, Inc.
2024-09-20
INFINITY
INFINITY
98737979 not registered Live/Pending
Marten Group, Inc.
2024-09-06
INFINITY
INFINITY
98643936 not registered Live/Pending
Project Management Institute, Inc.
2024-07-11
INFINITY
INFINITY
98470220 not registered Live/Pending
IBF IP, LLC
2024-03-27
INFINITY
INFINITY
98466286 not registered Live/Pending
IBF IP, LLC
2024-03-25
INFINITY
INFINITY
98454204 not registered Live/Pending
Tanks By Mail Inc
2024-03-18
INFINITY
INFINITY
98433629 not registered Live/Pending
Infinity Generation Inc.
2024-03-05
INFINITY
INFINITY
98338571 not registered Live/Pending
Careismatic Brands, LLC
2024-01-02
INFINITY
INFINITY
98293120 not registered Live/Pending
PREFERRED COLLECTIONS INC.
2023-11-30
INFINITY
INFINITY
98275942 not registered Live/Pending
Capital One Financial Corporation
2023-11-17
INFINITY
INFINITY
98242984 not registered Live/Pending
IGH Holding Inc.
2023-10-27
INFINITY
INFINITY
98175956 not registered Live/Pending
CellFE, Inc.
2023-09-12
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