| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00841523155903 | Tesera-k ALIF | 2167-002-001 | Straight Punch Awl | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 2 | 00841523155606 | Tesera-k ALIF | 2167-000-056 | Size 4 Cup Curette | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 3 | 00841523155590 | Tesera-k ALIF | 2167-000-054 | Size 2 Cup Curette | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 4 | 00841523160488 | Tesera-k ALIF | 2167-013-001 | Angled Cover Plate Inserter | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 5 | 00841523155583 | Tesera-k ALIF | 2167-000-031 | Endplate Perforator Tool | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 6 | 00841523160471 | Tesera-k ALIF | 2167-011-003 | Angled Tesera-k ALIF Cage Inserter | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 7 | 00841523155699 | Tesera-k ALIF | 2167-000-074 | 13mm Endplate Rasp | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 8 | 00841523155576 | Tesera-k ALIF | 2167-000-030 | 90° Ball Tip Probe | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 9 | 00841523158393 | Tesera-k ALIF | 2167-012-015 | Angled Retaining Hex Driver | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 10 | 00841523158355 | Tesera-k ALIF | 3167-006-000 | 27x24 Tesera-k A ALIF Instrument Case | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 11 | 00841523155569 | Tesera-k ALIF | 2167-000-027 | 6mm Kerrison Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 12 | 00841523158348 | Tesera-k ALIF | 2168-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 13 | 00841523158331 | Tesera-k ALIF | 2168-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 14 | 00841523158324 | Tesera-k ALIF | 2168-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 15 | 00841523158317 | Tesera-k ALIF | 2168-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 16 | 00841523158300 | Tesera-k ALIF | 2168-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 17 | 00841523158294 | Tesera-k ALIF | 2168-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 18 | 00841523155552 | Tesera-k ALIF | 2167-000-026 | 3mm Kerrison Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 19 | 00841523158287 | Tesera-k ALIF | 2168-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 20 | 00841523158270 | Tesera-k ALIF | 2168-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 21 | 00841523158263 | Tesera-k ALIF | 2168-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 22 | 00841523157860 | Tesera-k ALIF | 3167-004-000 | Tesera-k ALIF Trial Case | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 23 | 00841523158256 | Tesera-k ALIF | 2168-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 24 | 00841523158249 | Tesera-k ALIF | 2167-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 25 | 00841523158232 | Tesera-k ALIF | 2167-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 26 | 00841523158225 | Tesera-k ALIF | 2167-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 27 | 00841523158218 | Tesera-k ALIF | 2167-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 28 | 00841523158201 | Tesera-k ALIF | 2167-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 29 | 00841523155545 | Tesera-k ALIF | 2167-000-025 | 8mm Pituitary Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 30 | 00841523158195 | Tesera-k ALIF | 2167-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 31 | 00841523155538 | Tesera-k ALIF | 2167-000-024 | 4mm Pituitary Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 32 | 00841523158188 | Tesera-k ALIF | 2167-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 33 | 00841523158171 | Tesera-k ALIF | 2167-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 34 | 00841523158164 | Tesera-k ALIF | 2167-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 35 | 00841523155521 | Tesera-k ALIF | 2167-000-023 | 10mm Sypert Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 36 | 00841523158157 | Tesera-k ALIF | 2167-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 37 | 00841523158140 | Tesera-k ALIF | 2167-134-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 12° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 38 | 00841523158133 | Tesera-k ALIF | 2167-131-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 12° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 39 | 00841523158126 | Tesera-k ALIF | 2167-042-209 | Tesera-k ALIF, 42W X 32D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 40 | 00841523155514 | Tesera-k ALIF | 2167-000-022 | 5mm Sypert Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 41 | 00841523155507 | Tesera-k ALIF | 2167-000-021 | Scalpel Handle | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 42 | 00841523155491 | Tesera-k ALIF | 2167-000-004 | 42W x 32D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 43 | 00841523158119 | Tesera-k ALIF | 2167-038-009 | Tesera-k ALIF, 38W X 30D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 44 | 00841523158102 | Tesera-k ALIF | 2167-034-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 45 | 00841523158096 | Tesera-k ALIF | 2167-031-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 46 | 00841523158072 | Tesera-k ALIF | 2167-000-000 | 27W x 24D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 47 | 00841523158065 | Tesera-k ALIF | 2167-001-008 | Tesera-k A ALIF 27W x 24D Oblique Cage Inserter Tip | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 48 | 00841523155484 | Tesera-k ALIF | 2167-000-003 | 38W x 30D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 49 | 00841523158058 | Tesera-k ALIF | 2167-001-007 | Tesera-k A ALIF Oblique Cage Inserter Tip | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 50 | 00841523155477 | Tesera-k ALIF | 2167-000-002 | 34W x 28D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 28031497001900 | SPK0722 | Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. | Interspace Knee ATS 80/12 | TECRES SPA | |
| 2 | 28031497001894 | SPK0622 | Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. | Interspace Knee ATS 80/07 | TECRES SPA | |
| 3 | 28031497001887 | SPK0522 | Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement.The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. | Interspace Knee ATS 60/12 | TECRES SPA | |
| 4 | 28031497001870 | SPK0422 | Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. | Interspace Knee ATS 60/07 | TECRES SPA | |
| 5 | 28031497001160 | SPK0322 | Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process.InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/polymethylmethacrylate), Interspace Knee is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. | InterSpace Knee | TECRES SPA | |
| 6 | 28031497000606 | SPK0222 | Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Knee | TECRES SPA | |
| 7 | 28031497000590 | SPK0122 | Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Knee | TECRES SPA | |
| 8 | 28031497000583 | SPK0022 | Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). | InterSpace Knee | TECRES SPA | |
| 9 | 10885862621931 | SPI-046699 | SPI-046699 | Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block | Truliant | EXACTECH, INC. |
| 10 | 10885862621924 | SPI-046300 | SPI-046300 | Special Pinned Femoral LT-INT / RT- EXT Rotation Adjustment Block | Truliant | EXACTECH, INC. |
| 11 | 10885862621528 | SPI-046441 | SPI-046441 | SPECIAL VAN DE LEUR TIBIAL RESECTOR, UPPER ASSEMBLY | Truliant | EXACTECH, INC. |
| 12 | 10885862618719 | SPI-046412 | SPI-046412 | SPECIAL LPI TIBIAL RESECETION BLOCK, RIGHT, WIDE SLOT | Truliant | EXACTECH, INC. |
| 13 | 10885862618702 | SPI-046411 | SPI-046411 | SPECIAL LPI TIBIAL RESECETION BLOCK, LEFT, WIDE SLOT | Truliant | EXACTECH, INC. |
| 14 | 10885862618214 | SPI-046319 | SPI-046319 | Truliant | EXACTECH, INC. | |
| 15 | 10885862618207 | SPI-046022 | SPI-046022 | SPECIAL VAN DE LEUR TIBIAL RESECTOR, SHAFT ASSEMBLY | Truliant | EXACTECH, INC. |
| 16 | 10885862618146 | SPI-046017 | SPI-046017 | SPECIAL VAN DE LEUR TIBIAL RESECTOR, ANKLE YOKE | Truliant | EXACTECH, INC. |
| 17 | 10885862617989 | SPI-038032-60 | SPI-038032-60 | Truliant | EXACTECH, INC. | |
| 18 | 10885862617972 | SPI-045747-35 | SPI-045747-35 | Truliant | EXACTECH, INC. | |
| 19 | 10885862617965 | SPI-045745-29 | SPI-045745-29 | Truliant | EXACTECH, INC. | |
| 20 | 10885862617668 | SPI-045404 | SPI-045404 | Truliant | EXACTECH, INC. | |
| 21 | 10885862617453 | SPI-044689 | SPI-044689 | Truliant | EXACTECH, INC. | |
| 22 | 10885862617217 | SPI-044794 | SPI-044794 | Truliant | EXACTECH, INC. | |
| 23 | 10885862617132 | SPI-044447 | SPI-044447 | Truliant | EXACTECH, INC. | |
| 24 | 10885862610195 | SPI-044406 | SPI-044406 | Truliant | EXACTECH, INC. | |
| 25 | 10885862606884 | SPI-041553-32 | SPI-041553-32 | Truliant | EXACTECH, INC. | |
| 26 | 10885862606877 | SPI-041550-5 | SPI-041550-5 | Truliant | EXACTECH, INC. | |
| 27 | 10885862606860 | SPI-041550-4 | SPI-041550-4 | Truliant | EXACTECH, INC. | |
| 28 | 10885862606853 | SPI-041550-3 | SPI-041550-3 | Truliant | EXACTECH, INC. | |
| 29 | 10885862606846 | SPI-041550-2 | SPI-041550-2 | Truliant | EXACTECH, INC. | |
| 30 | 10885862606839 | SPI-041550-1 | SPI-041550-1 | Truliant | EXACTECH, INC. | |
| 31 | 10885862605672 | SPI-040853 | SPI-040853 | Truliant | EXACTECH, INC. | |
| 32 | 10885862605665 | SPI-040844 | SPI-040844 | Truliant | EXACTECH, INC. | |
| 33 | 10885862605542 | SPI-040738 | SPI-040738 | Truliant | EXACTECH, INC. | |
| 34 | 10885862603579 | SPI-040344 | SPI-040344 | Truliant | EXACTECH, INC. | |
| 35 | 10885862603562 | SPI-040343 | SPI-040343 | Truliant | EXACTECH, INC. | |
| 36 | 10885862603203 | SPI-040152 | SPI-040152 | Truliant | EXACTECH, INC. | |
| 37 | 10885862603128 | SPI-039661-60 | SPI-039661-60 | Truliant | EXACTECH, INC. | |
| 38 | 10885862603111 | SPI-039661-50 | SPI-039661-50 | Truliant | EXACTECH, INC. | |
| 39 | 10885862603104 | SPI-039661-45 | SPI-039661-45 | Truliant | EXACTECH, INC. | |
| 40 | 10885862603098 | SPI-039661-40 | SPI-039661-40 | Truliant | EXACTECH, INC. | |
| 41 | 10885862603081 | SPI-039661-35 | SPI-039661-35 | Truliant | EXACTECH, INC. | |
| 42 | 10885862603074 | SPI-039661-30 | SPI-039661-30 | Truliant | EXACTECH, INC. | |
| 43 | 10885862603067 | SPI-039661-25 | SPI-039661-25 | Truliant | EXACTECH, INC. | |
| 44 | 10885862603050 | SPI-039661-20 | SPI-039661-20 | Truliant | EXACTECH, INC. | |
| 45 | 10885862603043 | SPI-039661-15 | SPI-039661-15 | Truliant | EXACTECH, INC. | |
| 46 | 10885862603036 | SPI-039661-10 | SPI-039661-10 | Truliant | EXACTECH, INC. | |
| 47 | 10885862603029 | SPI-039661-00 | SPI-039661-00 | Truliant | EXACTECH, INC. | |
| 48 | 10885862603012 | SPI-039670-R | SPI-039670-R | Truliant | EXACTECH, INC. | |
| 49 | 10885862603005 | SPI-039670-L | SPI-039670-L | Truliant | EXACTECH, INC. | |
| 50 | 10885862602589 | SPI-039616 | SPI-039616 | Truliant | EXACTECH, INC. |