| Primary Device ID | 00888867052925 | 
| NIH Device Record Key | 0f9196dd-480d-48d3-a38d-5e933f2eab9c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Arthrex® | 
| Version Model Number | AR-8944CL-S | 
| Catalog Number | AR-8944CL-S | 
| Company DUNS | 131747628 | 
| Company Name | ARTHREX, 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 | 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 | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | |
| Phone | +1(800)934-4404 | 
| complaints@arthrex.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00888867052925 [Primary] | 
| HIBCC | M150AR8944CLS0 [Secondary] | 
| HRS | PLATE, FIXATION, BONE | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
[00888867052925]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 14 | 
| Public Version Date | 2020-03-05 | 
| Device Publish Date | 2017-02-15 | 
| 10888867084008 | ANGEL cPRP PROCESSING SET US | 
| 10888867020808 | DISP INSTR. KIT FOR TENO SCRW | 
| 10888867018645 | DISPS KIT FOR 3X 8MM TENO | 
| M150AR8942RLS1 | H-PLATE, 36 X 16MM RIGHT, LARGE, STRL | 
| M150AR8942LMS1 | H-PLATE, 32 X 16MM, LEFT, MED, STRL | 
| 00888867020771 | IMPL SYS,LAT ANKLE RECON | 
| 00888867008786 | TIB OPEN WEDGE OSTEO PLATE, 17.5 MM | 
| 00888867008762 | TIB OPEN WEDGE OSTEO PLATE, 16 MM | 
| 00888867008724 | TIB OPEN WEDGE OSTEO PLATE, 13.5 MM | 
| 00888867008700 | TIB OPEN WEDGE OSTEO PLATE, 12.5 MM | 
| 00888867008663 | TIB OPEN WEDGE OSTEO PLATE, 10 MM | 
| 00888867008649 | TIB OPEN WEDGE OSTEO PLATE, 9 MM | 
| 00888867008625 | TIB OPEN WEDGE OSTEO PLATE, 7.5 MM | 
| 00888867008601 | TIB OPEN WEDGE OSTEO PLATE, 6 MM | 
| 00888867008588 | TIB OPEN WEDGE OSTEO PLATE, 5 MM | 
| 00888867007581 | FEM OPENG WEDG OSTEO PLT,12.5MM | 
| 00888867007543 | FEM OPENG WEDG OSTEO PLT,10MM | 
| 00888867007505 | FEM OPENG WEDG OSTEO PLT,7.5MM | 
| M150AR8951LRS1 | LISFRANC PLATE, LARGE, RIGHT,TI, STRL | 
| M150AR8951MRS1 | LISFRANC PLATE, MEDIUM,RIGHT,TI, STRL | 
| M150AR8951SRS1 | LISFRANC PLATE, SMALL, RIGHT TI, STRL | 
| M150AR8951LLS1 | LISFRANC PLATE, LARGE, LEFT, TI, STRL | 
| M150AR8951MLS1 | LISFRANC PLATE, MEDIUM, LEFT,TI, STRL | 
| M150AR8951SLS1 | LISFRANC PLATE, SMALL, LEFT, TI, STRL | 
| 00888867009608 | 17.5 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009585 | 16MM, TIBIAL A/P SLOPED OSTEOTOMY PLATE | 
| 00888867009561 | 15 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009547 | 13.5MMTIB A/P SLPD OSTEO PLT | 
| 00888867009523 | 12.5 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009509 | 11.0 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009462 | 9 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009448 | 7.5 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| 00888867009424 | 6MM, TIBIAL A/P SLOPED OSTEOTOMY PLATE | 
| 00888867009400 | 5 MM TIBIAL A/P SLOPED OSTEO PLATE | 
| M150AR700040FTS1 | CANN SCRW 3.75X 40MMFULLY THRDED, STRL | 
| M150AR700028FTS1 | CANN SCRW,3.75X 28MMFULLY THRDED, STRL | 
| M150AR700026FTS1 | CANN SCRW,3.75X 26MMFULLY THRDED, STRL | 
| M150AR8916VNC34S1 | 2.4X34MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC32S1 | 2.4X32MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC30S1 | 2.4X30MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC28S1 | 2.4X28MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC26S1 | 2.4X26MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC24S1 | 2.4X24MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC22S1 | 2.4X22MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC20S1 | 2.4X20MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC18S1 | 2.4X18MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC16S1 | 2.4X16MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC14S1 | 2.4X14MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC12S1 | 2.4X12MM VAL NEAR CORTEX SCREW, Ti, STRL | 
| M150AR8916VNC10S1 | 2.4X10MM VAL NEAR CORTEX SCREW,Ti, STRL | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() ARTHREX  87595305  5598566 Live/Registered  | 
        Arthrex, Inc.  2017-09-04  | 
![]() ARTHREX  87595302  5598565 Live/Registered  | 
        Arthrex, Inc.  2017-09-04  | 
![]() ARTHREX  85078407  3911238 Live/Registered  | 
        Arthrex, Inc.  2010-07-06  | 
![]() ARTHREX  74317485  1788030 Live/Registered  | 
        ARTHREX INC.  1992-09-24  | 
![]() ARTHREX  74128118  not registered Dead/Abandoned  | 
        Arthrex Arthroscopy Instruments, Inc.  1991-01-04  | 
![]() ARTHREX  73436631  1328327 Dead/Cancelled  | 
        Surgical Equipment Associates, Ltd.  1983-07-28  | 
![]() ARTHREX  73281788  1191044 Dead/Cancelled  | 
        Gerchenson; Emile H.  1980-10-14  |