| Primary Device ID | 03663136027630 | 
| NIH Device Record Key | 79b2a96f-6dea-432d-93ae-69b87e8dc359 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | LUMIS™ | 
| Version Model Number | MS1-R6035T | 
| Company DUNS | 390377518 | 
| Company Name | SPINEVISION | 
| 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 | true | 
| OTC Over-The-Counter | false | 
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | |
| Phone | +33153332525 | 
| Corp.quality@spinevision.com | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Outer Diameter | 6 Millimeter | 
| Length | 35 Millimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 03663136027630 [Primary] | 
| KWQ | Appliance, Fixation, Spinal Intervertebral Body | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
[03663136027630]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2025-01-09 | 
| Device Publish Date | 2016-05-18 | 
| 03663136020181 | Ti 6.0 mm x 135 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136018782 | Ø8mm CANNULATED TAP | 
| 03663136007809 | MULTI-AXIAL SCREW Ø 8.5mm L 60mm | 
| 03663136007670 | MULTI-AXIAL SCREW Ø 6.5mm L 55mm | 
| 03663136006949 | MULTI-AXIAL SCREW, DIAMETER 5.5mm, LENGTH 45mm | 
| 03663136006925 | MULTI-AXIAL SCREW, DIAMETER 5.5mm, LENGTH 35mm | 
| 03663136007793 | MULTI-AXIAL SCREW Ø 8.5mm L 55mm | 
| 03663136007724 | MULTI-AXIAL SCREW Ø 7.5mm L 50mm | 
| 03663136007595 | MULTI-AXIAL SCREW Ø 5.5mm L 45mm | 
| 03663136007540 | GUIDE WIRE DIAMETER 1.4mm, LENGTH 500mm | 
| 03663136007366 | Ti 6.0 mm x 100 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136007335 | Ti 6.0 mm x 85 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136007274 | Ti 6.0 mm x 70 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136006987 | MULTI-AXIAL SCREW, DIAMETER 6.5mm, LENGTH 40mm | 
| 03663136006628 | INDEX RING FOR SETSCREW HOLDER | 
| 03663136006611 | SETSCREW HOLDER | 
| 03663136007755 | MULTI-AXIAL SCREW Ø 8.5mm L35mm | 
| 03663136027654 | Prebent percutaneous rod 6.0mm x 35mm | 
| 03663136027647 | Prebent percutaneous rod 6.0mm x 30mm | 
| 03663136027630 | Straight percutaneous rod 6.0mm x 35mm | 
| 03663136027623 | Straight percutaneous rod 6.0mm x 30mm | 
| 03663136023670 | LUMIS™ INSERT FOR INSTRUMENTS | 
| 03663136020174 | Ti 6.0 mm x 125 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136020167 | Ti 6.0 mm x 115 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136020150 | Ti 6.0 mm x 105 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136020143 | Ti 6.0 mm x 95 mm PRE-BENT PERCUTANEOUS ROD | 
| 03663136020136 | Ti 6.0 mm x 135 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136020129 | Ti 6.0 mm x 125 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136020112 | Ti 6.0 mm x 115 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136020105 | Ti 6.0 mm x 105 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136020099 | Ti 6.0 mm x 95 mm STRAIGHT PERCUTANEOUS ROD | 
| 03663136020082 | MULTI-AXIAL SCREW, DIAMETER 6.5mm, LENGTH 60mm | 
| 03663136008172 | MOFALSEBLOC SCREW, Ø 8.5mm, L 90mm | 
| 03663136008165 | MOFALSEBLOC SCREW, Ø 8.5mm, L 85mm | 
| 03663136008158 | MOFALSEBLOC SCREW, Ø 8.5mm, L 80mm | 
| 03663136008141 | MOFALSEBLOC SCREW, Ø 8.5mm, L 75mm | 
| 03663136008103 | MOFALSEBLOC SCREW, Ø 8.5mm, L 55mm | 
| 03663136008097 | MOFALSEBLOC SCREW, Ø 8.5mm, L 50mm | 
| 03663136008073 | MOFALSEBLOC SCREW, Ø 8.5mm, L 40mm | 
| 03663136008066 | MOFALSEBLOC SCREW, Ø 8.5mm, L 35mm | 
| 03663136008059 | MOFALSEBLOC SCREW, Ø 7.5mm, L 60mm | 
| 03663136008042 | MOFALSEBLOC SCREW, Ø 7.5mm, L 55mm | 
| 03663136008035 | LUMIS™MOFALSEBLOC SCREW, Ø 7.5mm, L 50mm | 
| 03663136008028 | MOFALSEBLOC SCREW, Ø 7.5mm, L 45mm | 
| 03663136008011 | MOFALSEBLOC SCREW, Ø 7.5mm, L 40mm | 
| 03663136007991 | MOFALSEBLOC SCREW, Ø 6.5mm, L 60mm | 
| 03663136007984 | MOFALSEBLOC SCREW, Ø 6.5mm, L 55mm | 
| 03663136007977 | MOFALSEBLOC SCREW, Ø 6.5mm, L 50mm | 
| 03663136007960 | MOFALSEBLOC SCREW, Ø 6.5mm, L 45mm | 
| 03663136007953 | MOFALSEBLOC SCREW, Ø 6.5mm, L 40mm | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() LUMIS  98749003  not registered Live/Pending  | 
        JV Eighteen LLC  2024-09-13  | 
![]() LUMIS  98497161  not registered Live/Pending  | 
        Jekabs Otankis  2024-04-12  | 
![]() LUMIS  97723392  not registered Live/Pending  | 
        Lumis Corp  2022-12-19  | 
![]() LUMIS  90252344  not registered Live/Pending  | 
        Lumis Group LLC  2020-10-13  | 
![]() LUMIS  90252294  not registered Live/Pending  | 
        Lumis Group LLC  2020-10-13  | 
![]() LUMIS  87870684  not registered Live/Pending  | 
        SS&C Technologies, Inc.  2018-04-10  | 
![]() LUMIS  86139443  4697031 Live/Registered  | 
        RESMED PTY LTD  2013-12-10  | 
![]() LUMIS  85719352  not registered Dead/Abandoned  | 
        LUMINATION LLC  2012-09-03  | 
![]() LUMIS  79092308  4047593 Live/Registered  | 
        Spinevision  2010-12-03  | 
![]() LUMIS  76245075  not registered Dead/Abandoned  | 
        BRISTOL-MYERS SQUIBB PHARMA COMPANY  2001-04-23  | 
![]() LUMIS  75677267  not registered Dead/Abandoned  | 
        McCullough, William  1999-04-10  |