Titan™ DRG092206701
GUDID M269DRG0922067011
Titan™ Total Shoulder System The glenoid drill guide is used for precision and accuracy when drilling.
Ascension Orthopedics, Inc.
Surgical drill guide, reusable| Primary Device ID | M269DRG0922067011 |
| NIH Device Record Key | f46a43cf-f99c-4a43-9cb2-455de6341d2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Titan™ |
| Version Model Number | DRG-0922-067-01 |
| Catalog Number | DRG092206701 |
| Company DUNS | 942377524 |
| Company Name | Ascension Orthopedics, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com | |
| Phone | +1(800)654-2873 |
| custsvcnj@integralife.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10381780244547 [Primary] |
| HIBCC | M269DRG0922067011 [Secondary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
[M269DRG0922067011]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2017-08-30 |
On-Brand Devices [Titan™]
| 10381780471288 | RSS Glenosphere Removal Handle-S |
| 10381780459118 | RSS Reamer Guide Body Inserter/Extractor |
| 10381780459101 | RSS Humeral Body Inserter/Extractor |
| M269SEP09200680011 | Titan™ Total Shoulder System The body separator is used in the removal of the proximal humeral |
| M269INS0960049011 | Titan™ Reverse Shoulder System The reamer guide body inserter/extractor is used to assist with |
| M269IS09500450011 | The humeral implant inserter/extractor is used to insert the implant into its place, as well as |
| M269INS0960048021 | The humeral body inserter/extractor knob is used to tighten or loosen the inserter/extractor. |
| M269INS0960048011 | The humeral body inserter/extractor is used to insert the implant into its place, as well as ext |
| M269HDL0960065011 | The glenosphere inserter is used to insert the glenosphere into the baseplate. |
| M269SET188A0011 | The head extractor is used to remove the humeral head. |
| M269INS09500460011 | The humeral trial inserter/extractor is used to insert the trial implant into its place, as well |
| M269INS09230460011 | The humeral trial inserter/extractor is used to insert the trial implant into its place, as well |
| M269INS09230450011 | The humeral implant inserter/extractor is used to insert the implant into its place, as well as |
| M269INS09200460011 | The humeral trial inserter/extractor is used to insert the trial implant into its place, as well |
| M269INS09200450011 | The humeral implant inserter/extractor is used to insert the implant into its place, as well as |
| M269GLN092603003A1 | The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg t |
| M269GLN092603002A1 | The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg t |
| M269GLN092603001A1 | The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg t |
| M269GLN092603000A1 | The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg t |
| 10381780467601 | RSS HXL Liner Retentive, +9R |
| 10381780467595 | RSS HXL Liner Retentive, +6R |
| 10381780467588 | RSS HXL Liner Retentive, +3R |
| 10381780467571 | RSS HXL Liner Retentive, +0R |
| 10381780467564 | RSS HXL Liner Standard, +9S |
| 10381780467557 | RSS HXL Liner Standard, +6S |
| 10381780467540 | RSS HXL Liner Standard, +3S |
| 10381780467533 | RSS HXL Liner Standard, +0S |
| M269IMS0960070011 | Titan™ Reverse Shoulder System The stand is used as a base during stem impaction. |
| M269SCR0960062011 | Titan™ Reverse Shoulder System The 2.5 Hex Driver is used to tighten 4.5mm screws. |
| 10381780467779 | RSS Double Drill Guide-S |
| 10381780467762 | RSS Baseplate Boss Drill Guide-S |
| M269DRS09260011 | The Glenoid Drill Shaft is used to create holes. |
| M269DRL0926018S1 | Fin-Lock Central Drill |
| M269DRL0926018C1 | Fin-Lock Cannulated Central Drill |
| M269DRL0926015S1 | Fin-Lock Central Drill |
| M269DRL0926015C1 | Fin-Lock Cannulated Central Drill |
| M269DRL09260021 | Fin-Lock Peripheral Drill |
| M269DRL09260011 | Fin-Lock Starter Drill |
| M269DRG09260031 | Fin-Lock Starter Drill Guide |
| M269DRG09260021 | Fin-Lock Starter Drill Guide |
| M269DRG09260011 | The Fin-Lock Drill Guide is used for precision and accuracy when drilling. |
| M269STD09200710011 | Titan™ Total Shoulder System The stand is used as a base during head impaction. |
| M269SIS09200540011 | Titan™ Total Shoulder System The stand is used as a base during stem impaction. |
| M269INS0920071STD1 | Titan™ Total Shoulder System The stand insert is used as a base during head impaction. |
| M269INS0920071SML1 | Titan™ Total Shoulder System The stand insert is used as a base during head impaction. |
| M269INS0920071LRG1 | Titan™ Total Shoulder System The stand insert is used as a base during head impaction. |
| M269DRG0922067021 | Titan™ Total Shoulder System The glenoid drill guide is used for precision and accuracy when d |
| M269DRG0922067011 | Titan™ Total Shoulder System The glenoid drill guide is used for precision and accuracy when d |
| M269DRG09200490021 | Titan™ Total Shoulder System The center glenoid drill guide is used for precision and accuracy |
| M269DRG09200490011 | Titan™ Total Shoulder System The center glenoid drill guide is used for precision and accuracy |
Trademark Results [Titan]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 TITAN 98804197 not registered Live/Pending |
Star Asia U.S.A. LLC 2024-10-16 |
 TITAN 98782018 not registered Live/Pending |
TITAN CHAIR LLC 2024-10-02 |
 TITAN 98752443 not registered Live/Pending |
ReCreate Holdings LLC 2024-09-16 |
 TITAN 98686836 not registered Live/Pending |
Emecole Metro, LLC 2024-08-07 |
 TITAN 98648191 not registered Live/Pending |
Hausmann Enterprises LLC 2024-07-15 |
 TITAN 98641947 not registered Live/Pending |
PRODUCE IN PARADISE, INC. 2024-07-10 |
 TITAN 98641943 not registered Live/Pending |
PRODUCE IN PARADISE, INC. 2024-07-10 |
 TITAN 98622484 not registered Live/Pending |
Accela Group LLC 2024-06-27 |
 TITAN 98622467 not registered Live/Pending |
Accela Group LLC 2024-06-27 |
 TITAN 98607114 not registered Live/Pending |
Giebitz, Aaron 2024-06-18 |
 TITAN 98591448 not registered Live/Pending |
Longhui Yuan 2024-06-07 |
 TITAN 98567109 not registered Live/Pending |
Titan Wellness Systems Inc. 2024-05-24 |
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