| Primary Device ID | 00763000713126 |
| NIH Device Record Key | 2c4838d4-ef6e-4568-894e-47c9d8f374ae |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ModuLeX™ Shank Mount |
| Version Model Number | 9736438 |
| Company DUNS | 835233107 |
| Company Name | MEDTRONIC NAVIGATION, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000713126 [Primary] |
| OLO | Orthopedic stereotaxic instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
[00763000713126]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-28 |
| Device Publish Date | 2025-07-19 |
| 00763000713126 | MODULEX SHANK MOUNT RIGHT 9736438 |
| 00763000713119 | MODULEX SHANK MOUNT LEFT 9736437 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MODULEX 88911657 not registered Live/Pending |
WARSAW ORTHOPEDIC, INC. 2020-05-12 |
![]() MODULEX 79309623 not registered Live/Pending |
The Product Makers (Australia) Pty Limited 2020-09-24 |
![]() MODULEX 78914223 3451320 Live/Registered |
UNICAL AG S.P.A. 2006-06-22 |
![]() MODULEX 76515852 3181296 Live/Registered |
MODULEX INC. 2003-05-21 |
![]() MODULEX 74505041 1916317 Dead/Cancelled |
Computerized Medical Systems, Inc. 1994-03-25 |
![]() MODULEX 74385203 1827226 Dead/Expired |
FLEETWOOD SYSTEMS, INC. 1993-04-28 |
![]() MODULEX 73405892 1343780 Live/Registered |
A/S MODULEX 1982-12-13 |
![]() MODULEX 73193269 not registered Dead/Abandoned |
FEDOR EXPOSITIONS, INC. 1978-11-14 |
![]() MODULEX 73101282 1065780 Dead/Cancelled |
Modular Fixtures Corporation 1976-09-27 |
![]() MODULEX 73045750 1086248 Dead/Expired |
A/S MODULEX 1975-03-04 |
![]() MODULEX 72178295 0794016 Dead/Expired |
A/S MODULEX 1963-10-03 |
![]() MODULEX 72145854 0745172 Dead/Expired |
RITTER COMPANY, INC. 1962-05-31 |