Other products from "SHALBY ADVANCED TECHNOLOGIES, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00840286802024 1009-0-0012 Proximal Spacer, 12 JDL Prosthesis, hip, semi-constrained (metal cemented acetabular component) 3 Consensus Hip System
2 00840286802017 1009-0-0011 Proximal Spacer, 11 JDL Prosthesis, hip, semi-constrained (metal cemented acetabular component) 3 Consensus Hip System
3 00840286839686 CKSCOND4 CKSCOND4 CKS Condensed System Case 4 LXH Orthopedic manual surgical instrument 1 CKSCOND4
4 00840286839556 TAPERSETCASE1 TAPERSETCASE1 Taperset Case 1 LXH Orthopedic manual surgical instrument 1 TAPERSETCASE1
5 00840286839471 RKSCASE1 RKSCASE1 General Instruments LXH Orthopedic manual surgical instrument 1 RKSCASE1
6 00840286803564 1017-1-2043 1017-1-2043 Unipolar Head, 43mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
7 00840286803557 1017-1-2042 1017-1-2042 Unipolar Head, 42mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
8 00840286803540 1017-1-2041 1017-1-2041 Unipolar Head, 41mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
9 00840286803533 1017-1-2040 1017-1-2040 Unipolar Head, 40mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
10 00840286803281 1017-0-2059 1017-0-2059 Unipolar Head, 59mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
11 00840286802338 1010-3-0016 Femoral Stem, Collared, Cemented, 16 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
12 00840286802321 1010-3-0015 Femoral Stem, Collared, Cemented, 15 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
13 00840286802314 1010-3-0014 Femoral Stem, Collared, Cemented, 14 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
14 00840286803717 1017-1-2058 1017-1-2058 Unipolar Head, 58mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
15 00840286803700 1017-1-2057 1017-1-2057 Unipolar Head, 57mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
16 00840286802307 1010-3-0013 Femoral Stem, Collared, Cemented, 13 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
17 00840286802291 1010-3-0012 Femoral Stem, Collared, Cemented, 12 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
18 00840286802284 1010-3-0011 Femoral Stem, Collared, Cemented, 11 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
19 00840286802277 1010-3-0010 Femoral Stem, Collared, Cemented, 10 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
20 00840286802260 1010-3-0009 Femoral Stem, Collared, Cemented, 9 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
21 00840286802253 1010-3-0008 Femoral Stem, Collared, Cemented, 8 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
22 00840286810081 1710-3-0016 1710-3-0016 Femoral Stem, Collared, Cementless, PC, 16 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
23 00840286810074 1710-3-0015 1710-3-0015 Femoral Stem, Collared, Cementless, PC, 15 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
24 00840286802246 1010-2-0016 Femoral Stem, Collared, Cemented, 16 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
25 00840286810067 1710-3-0014 1710-3-0014 Femoral Stem, Collared, Cementless, PC, 14 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
26 00840286810050 1710-3-0013 1710-3-0013 Femoral Stem, Collared, Cementless, PC, 13 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
27 00840286810043 1710-3-0012 1710-3-0012 Femoral Stem, Collared, Cementless, PC, 12 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
28 00840286810036 1710-3-0011 1710-3-0011 Femoral Stem, Collared, Cementless, PC, 11 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
29 00840286810029 1710-3-0010 1710-3-0010 Femoral Stem, Collared, Cementless, PC, 10 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
30 00840286810012 1710-3-0009 1710-3-0009 Femoral Stem, Collared, Cementless, PC, 9 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
31 00840286810005 1710-3-0008 1710-3-0008 Femoral Stem, Collared, Cementless, PC, 8 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
32 00840286809993 1710-2-0016 1710-2-0016 Femoral Stem, Collared, Cementless, PC, 16 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
33 00840286809986 1710-2-0015 1710-2-0015 Femoral Stem, Collared, Cementless, PC, 15 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
34 00840286809979 1710-2-0014 1710-2-0014 Femoral Stem, Collared, Cementless, PC, 14 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
35 00840286809962 1710-2-0013 1710-2-0013 Femoral Stem, Collared, Cementless, PC, 13 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
36 00840286809955 1710-2-0012 1710-2-0012 Femoral Stem, Collared, Cementless, PC, 12 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
37 00840286809948 1710-2-0011 1710-2-0011 Femoral Stem, Collared, Cementless, PC, 11 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
38 00840286809931 1710-2-0010 1710-2-0010 Femoral Stem, Collared, Cementless, PC, 10 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
39 00840286809924 1710-2-0009 1710-2-0009 Femoral Stem, Collared, Cementless, PC, 9 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
40 00840286809917 1710-2-0008 1710-2-0008 Femoral Stem, Collared, Cementless, PC, 8 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
41 00840286809900 1710-0-0015 1710-0-0015 Femoral Stem, Collared, Cementless, PC, 15 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
42 00840286809894 1710-0-0014 1710-0-0014 Femoral Stem, Collared, Cementless, PC, 14 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
43 00840286809887 1710-0-0013 1710-0-0013 Femoral Stem, Collared, Cementless, PC, 13 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
44 00840286809870 1710-0-0012 1710-0-0012 Femoral Stem, Collared, Cementless, PC, 12 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
45 00840286809863 1710-0-0011 1710-0-0011 Femoral Stem, Collared, Cementless, PC, 11 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
46 00840286809856 1710-0-0010 1710-0-0010 Femoral Stem, Collared, Cementless, PC, 10 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
47 00840286809849 1710-0-0009 1710-0-0009 Femoral Stem, Collared, Cementless, PC, 9 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
48 00840286809832 1710-0-0008 1710-0-0008 Femoral Stem, Collared, Cementless, PC, 8 LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 Consensus Hip System
49 00840286803694 1017-1-2056 1017-1-2056 Unipolar Head, 56mm, +7mm KWL Prosthesis, hip, hemi-, femoral, metal 2 Consensus Hip System
50 00840286802239 1010-2-0015 Femoral Stem, Collared, Cemented, 15 LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 Consensus Hip System
Other products with the same Product Code "JWH"
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
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