Lattus LS-1001
GUDID 10889981298852
SHIM PUSHER, CENTER BLADE
SEASPINE ORTHOPEDICS CORPORATION
Orthopaedic prosthesis implantation instrument, reusable| Primary Device ID | 10889981298852 |
| NIH Device Record Key | bdfc8062-8206-451a-9945-00529235bca8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lattus |
| Version Model Number | LS-1001 |
| Catalog Number | LS-1001 |
| Company DUNS | 079840876 |
| Company Name | SEASPINE ORTHOPEDICS CORPORATION |
| 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 | false |
| 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(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com | |
| Phone | +1(760)727-8399 |
| custsvcspine@seaspine.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10889981298852 [Primary] |
FDA Product Code
| LXH | Orthopedic manual surgical instrument |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
[10889981298852]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-09-02 |
| Device Publish Date | 2022-08-25 |
On-Brand Devices [Lattus]
| 10889981300128 | 2-BLADE 22X180 LT |
| 10889981299095 | 2-BLADE 22X170 LT |
| 10889981299088 | 2-BLADE 22X160 LT |
| 10889981299071 | 2-BLADE 22X150 LT |
| 10889981299064 | 2-BLADE 22X140 LT |
| 10889981299057 | 2-BLADE 22X130 LT |
| 10889981299040 | 2-BLADE 22X120 LT |
| 10889981299033 | 2-BLADE 22X110 LT |
| 10889981299026 | 2-BLADE 22X100 LT |
| 10889981299019 | 2-BLADE 22X90 LT |
| 10889981299002 | 2-BLADE 22X180 RT |
| 10889981298999 | 2-BLADE 22X170 RT |
| 10889981298982 | 2-BLADE 22X160 RT |
| 10889981298975 | 2-BLADE 22X150 RT |
| 10889981298968 | 2-BLADE 22X140 RT |
| 10889981298951 | 2-BLADE 22X130 RT |
| 10889981298944 | 2-BLADE 22X120 RT |
| 10889981298937 | 2-BLADE 22X110 RT |
| 10889981298920 | 2-BLADE 22X100 RT |
| 10889981298913 | 2-BLADE 22X90 RT |
| 10889981298906 | TARGETING TOOL |
| 10889981298890 | LATTUS DILATOR HOLDER |
| 10889981298883 | CC SHIM REMOVAL TOOL |
| 10889981298876 | POSTERIOR SHIM REMOVAL TOOL |
| 10889981298869 | SHIM PUSHER, C/C |
| 10889981298852 | SHIM PUSHER, CENTER BLADE |
| 10889981298845 | THIN 4TH BLADE RETRACTOR 150MM |
| 10889981298838 | 4TH BLADE RETRACTOR 150MM |
| 10889981298821 | THIN 4TH BLADE RETRACTOR 200MM |
| 10889981298814 | 4TH BLADE RETRACTOR 200MM |
| 10889981307752 | Cephalad/Caudal 180mm Blade, AL |
| 10889981307745 | Cephalad/Caudal 170mm Blade, AL |
| 10889981307738 | Cephalad/Caudal 160mm Blade, AL |
| 10889981307721 | Cephalad/Caudal 150mm Blade, AL |
| 10889981307714 | Cephalad/Caudal 140mm Blade, AL |
| 10889981307707 | Cephalad/Caudal 130mm Blade, AL |
| 10889981307691 | Cephalad/Caudal 120mm Blade, AL |
| 10889981307684 | Cephalad/Caudal 110mm Blade, AL |
| 10889981307677 | Cephalad/Caudal 100mm Blade, AL |
| 10889981307660 | Cephalad/Caudal 90mm Blade, AL |
| 10889981307653 | Posterior Blade, SS, 180mm |
| 10889981307646 | Posterior Blade, SS, 170mm |
| 10889981307639 | Posterior Blade, SS, 160mm |
| 10889981307622 | Posterior Blade, SS, 150mm |
| 10889981307615 | Posterior Blade, SS, 140mm |
| 10889981307608 | Posterior Blade, SS, 130mm |
| 10889981307592 | Posterior Blade, SS, 120mm |
| 10889981307585 | Posterior Blade, SS, 110mm |
| 10889981307578 | Posterior Blade, SS, 100mm |
| 10889981307561 | Posterior Blade, SS, 90mm |
Trademark Results [Lattus]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LATTUS 88378374 not registered Live/Pending |
LATTUS, INC. 2019-04-09 |
 LATTUS 85654404 4590993 Live/Registered |
Quantum Corporation 2012-06-18 |
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