TenoLok T60A

GUDID 10845854043806

TenoLok 6.0mm Tenodesis Anchor

Conmed Corporation

Tendon/ligament bone anchor, non-bioabsorbable
Primary Device ID10845854043806
NIH Device Record Keyc05177cf-6c3e-4a20-bd2f-78f9af83b42c
Commercial Distribution StatusIn Commercial Distribution
Brand NameTenoLok
Version Model NumberT60A
Catalog NumberT60A
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com
Phone+1(866)426-6633
EmailCustomerExperience@conmed.com

Device Dimensions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS110845854043806 [Primary]
GS120845854043803 [Package]
Package: Carton [1 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBIFastener, fixation, nondegradable, soft tissue

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


[10845854043806]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-04-15
Device Publish Date2020-11-12

On-Brand Devices [TenoLok]

10845854044711T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
10845854044704T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit
10845854044681T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
10845854044667T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
20845854044671Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7
208458540437805.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture
20653405987182T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
20653405987175T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
20653405987168T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid
20653405987151T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit
10845854044698T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit
30845854044678Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7
308458540437875.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture
20653405987199T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit
10845854043806TenoLok 6.0mm Tenodesis Anchor
10845854043790TenoLok 6.0 mm Tenodesis Anchor with One #2 Hi-Fi Suture

Trademark Results [TenoLok]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TENOLOK
TENOLOK
86719830 4948048 Live/Registered
Conmed Corporation
2015-08-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.