| Primary Device ID | 10885862538062 | 
| NIH Device Record Key | 0803dba7-d647-4519-943a-66239fffdd72 | 
| Commercial Distribution Discontinuation | 2023-12-07 | 
| Commercial Distribution Status | Not in Commercial Distribution | 
| Brand Name | AcuMatch | 
| Version Model Number | 140-32-30 | 
| Catalog Number | 140-32-30 | 
| Company DUNS | 157565946 | 
| Company Name | Exactech, 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 | true | 
| Lot Batch | false | 
| Serial Number | true | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 10885862538062 [Primary] | 
| LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2025-08-28 | 
| Device Publish Date | 2018-03-20 | 
| 10885862616968 | SPI-044143-70 | 
| 10885862616951 | SPI-044143-68 | 
| 10885862616944 | SPI-044143-66 | 
| 10885862616920 | SPI-044143-62 | 
| 10885862616913 | SPI-044143-60 | 
| 10885862616906 | SPI-044143-58 | 
| 10885862616890 | SPI-044143-56 | 
| 10885862616883 | SPI-044143-54 | 
| 10885862616876 | SPI-044143-52 | 
| 10885862616869 | SPI-044143-50 | 
| 10885862616852 | SPI-044143-48 | 
| 10885862616845 | SPI-044143-46 | 
| 10885862616838 | SPI-044143-44 | 
| 10885862616821 | SPI-044143-42 | 
| 10885862096234 | ACUMATCH M-SERIES TEMPLATE SET | 
| 10885862096227 | M-SERIES 12/14 TEMPLATE | 
| 10885862096159 | P-SERIES COLLARED FEMORAL STEM TEMPLATE | 
| 10885862096142 | P-SERIES COLLARLESS FEMORAL STEM TEMPLATE | 
| 10885862096104 | C-SERIES CEM FEMORAL STEM TEMPLATE SET | 
| 10885862030597 | TEMPLATE, STEM, M-SERIES | 
| 10885862030573 | M-SERIES INSTRUMENT CASE 6 | 
| 10885862030566 | M-SERIES INSTRUMENT CASE 5 | 
| 10885862030559 | M-SERIES INSTRUMENT CASE 4 | 
| 10885862030542 | M-SERIES INSTRUMENT CASE 3 | 
| 10885862030535 | M-SERIES INSTRUMENT CASE 2 | 
| 10885862030528 | M-SERIES INSTRUMENT CASE 1 | 
| 10885862028907 | IMPACTOR ALIGNMENT GUIDE, M-SERIES | 
| 10885862028839 | NECK IMPACTOR, M-SERIES | 
| 10885862028822 | STEM IMPACTOR, M-SERIES | 
| 10885862028808 | OSTEOTOMY GUIDE, M-SERIES | 
| 10885862020482 | TEMPLATE, CUP, A-SERIES | 
| 10885862020444 | ACUMATCH REAMER TRAY | 
| 10885862020390 | ACUMATCH ACET. INST TRAY | 
| 10885862017420 | ACUMATCH FEMORAL INSTRUMENT TRAY #2 | 
| 10885862017413 | ACUMATCH FEMORAL INSTRUMENT TRAY #1 | 
| 10885862016072 | TEMPLATE, ACETABULAR CUP, ACUMATCH | 
| 10885862015570 | ACUMATCH BROACH HANDLE | 
| 10885862013101 | BIPOLAR INSTRUMENT CASE | 
| 10885862012807 | BIPOLAR ASSEMBLY PLIERS | 
| 10885862012791 | FEMORAL HEAD TEMPLATE, BIPOLAR | 
| 10885862012784 | TRIAL HANDLE ADAPTOR, BIPOLAR | 
| 10885862012777 | TRIAL HANDLE, BIPOLAR, ANGLED | 
| 10885862012760 | DISASSEMBLY TOOL, BIPOLAR | 
| 10885862012753 | TRIAL HANDLE, BIPOLAR, STRAIGHT | 
| 10885862012494 | TRIAL HANDLE ADAPTOR, BIPOLAR | 
| 10885862012180 | IMPACTOR, UNIPOLAR HEAD | 
| 10885862011008 | LINER EXTRACTOR, A-SERIES | 
| 10885862009616 | TEMPLATE, UNIPOLAR & BIPOLAR HEAD | 
| 10885862028945 | IMPACTOR, HEAD, M-SERIES | 
| 10885862028921 | EXTRACTOR HOOK, SMALL | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  ACUMATCH  85394374  not registered Dead/Abandoned | Atwood Technology Inc. 2011-08-10 | 
|  ACUMATCH  77917362  not registered Dead/Abandoned | Atwood Relationship Services Inc. 2010-01-21 | 
|  ACUMATCH  75754197  2360097 Live/Registered | Exactech, Inc. 1999-07-19 |