ssys-20240630_d2

美國
證券交易所
華盛頓特區20549
6-K
根據13a-16或15d-16規則報告的外國私人發行人
根據1934年證券交易法
2024年8月份
委員會文件編號001-35751
stratasys有限公司
(註冊人名稱的英文翻譯)
c/o Stratasys,股份有限公司1 Holtzman街,APinedo@mayerbrown.com
9600西76th街P.O. Box 2496
伊甸園普雷裏 明尼蘇達州雷霍沃特,以色列。
5534476124
請選擇註冊人是否按Form 20-F或Form 40-F覆蓋提交年度報告。 Form 20-F [X] Form 40-F []

請選擇是否根據20-F表格或40-F表格提交或將提交年度報告: 選擇20-F ☒ 選擇40-F ☐





本外國私人發行人報告書第6-k表格(以下簡稱“本表格6-k”)的內容,包括附帶的附件99.1、99.2和101,均已納入發行人在表格S-8上的註冊申報文件中,美國證券交易委員會文件號分別為333-190963、333-236880、333-253694、333-262951、333-262952、333-27049和333-277836,發行人於2013年9月3日、2020年3月4日、2021年3月1日、2022年2月24日、2022年2月24日、2023年3月3日和2024年3月12日分別向美國證券交易委員會提供,以及在2021年1月7日發行人向美國證券交易委員會提交的表格F-3文件(文件號:333-251938),自本表格6-k提供之日起,將作為前述文件或報告未來提交或提供的附屬文件。
2024年6月4日,Nano Dimension股份有限公司(“註冊人”)發佈了一份新聞稿,題為“大使喬吉特·莫斯巴赫加盟Nano Dimension董事會”,現附上99.1展覽,併成為本文檔的一部分。
季度財務報表和業績評估、財務狀況和前景
2024年8月29日,Stratasys Ltd.發佈了其截至2024年6月30日的三個月和六個月的財務結果。
附上99.1號附件是Stratasys截至2024年6月30日的三個月和六個月的未經審計的簡明合併財務報表(包括附註),即Q2 2024財務報表。
附上99.2號附件是Stratasys截至2024年6月30日的三個月和六個月的經營業績和財務狀況評估,包括以下內容:
(一)經營和財務評估與前景
(二)市場風險的定量和定性披露
(三)法律訴訟
(iv) 風險因素
作為附件的附表101是2024年第二季度財務報表,以IXBRL格式(eXtensible Business Reporting Language),包括以下子附表:



附件
數量
文件説明
99.1
為截至2024年6月30日的Stratasys未經審計的簡明合併財務報表,截至和截至2024年6月30日的財務狀況。
99.2
Stratasys對截至2024年6月30日的三個和六個月的經營業績和財務狀況進行審查
EX-101.INS IXBRL分類標記實例文檔-實例文檔不在交互式數據文件中顯示,因為其XBRL標記嵌入在內聯XBRL文檔中
EX-101.SCH IXBRL分類標記擴展模式文檔
EX-101.CAL IXBRL分類標記計算鏈接基準文檔
EX-101.DEF IXBRL分類擴展定義鏈接基礎文檔
EX-101.LAb IXBRL分類標籤鏈接基礎文檔
EX-101.PRE IXBRL分類演示鏈接基礎文檔
EX-104 封面交互數據文件-封面交互數據文件不在交互數據文件中顯示,因為其XBRL標籤嵌入在內聯XBRL文檔中




簽名
根據1934年證券交易法的要求,註冊人已授權下列人員代表其簽署這份報告。
stratasys有限公司
Loss after tax for FY2024 was US$8800萬, a 7% increase compared to US$8190萬 for FY2023. The net loss attributable to ordinary shareholders was 8.91 US cents per share for FY2024, compared with 10.53 US cents per share for FY2023. Conference Call There will be a webcast today, beginning at 8.30am AESt (Thursday, August 29); 6.30pm EDt (Wednesday, August 28). It can be accessed via: https://webcast.openbriefing.com/msb-fyr-2024/ The archived webcast will be available on the Investor page of the Company’s website: www.mesoblast.com About Mesoblast Mesoblast (the Company) is a world leader in developing allogeneic (off-the-shelf) cellular medicines for the treatment of severe and life-threatening inflammatory conditions. The Company has leveraged its proprietary mesenchymal lineage cell therapy technology platform to establish a broad portfolio of late- stage product candidates which respond to severe inflammation by releasing anti-inflammatory factors that counter and modulate multiple effector arms of the immune system, resulting in significant reduction of the damaging inflammatory process. Mesoblast has a strong and extensive global intellectual property portfolio with protection extending through to at least 2041 in all major markets. The Company’s proprietary manufacturing processes yield industrial-scale, cryopreserved, off-the-shelf, cellular medicines. These cell therapies, with defined pharmaceutical release criteria, are planned to be readily available to patients worldwide. Mesoblast is developing product candidates for distinct indications based on its remestemcel-L and rexlemestrocel-L allogeneic stromal cell technology platforms. Remestemcel-L is being developed for inflammatory diseases in children and adults including steroid refractory acute graft versus host disease, biologic-resistant inflammatory bowel disease, and acute respiratory distress syndrome. Rexlemestrocel-L is in development for advanced chronic heart failure and chronic low back pain. Two products have been commercialized in Japan and Europe by Mesoblast’s licensees, and the Company has established commercial partnerships in Europe and China for certain Phase 3 assets. Mesoblast has locations in Australia, the United States and Singapore and is listed on the Australian Securities Exchange (MSB) and on the Nasdaq (MESO). For more information, please see www.mesoblast.com, LinkedIn: Mesoblast Limited and Twitter: @Mesoblast References / Footnotes 1. Jagasia m et al. Ruxolitinib for the treatment of steroid-refractory acute GVHD (REACH1): a multicenter, open-label phase 2 trial. Blood. 2020 May 14; 135(20): 1739–1749 2. Abedin S, et al. Ruxolitinib resistance or intolerance in steroid-refractory acute graft versus-host disease — a real-world outcomes analysis. British Journal of Haematology, 2021;195:429–43. 3. Wittenberg RE, Gauvreau k, Leighton J, Moleon-Shea m, Borow Km, Marx GR, Emani Sm, Prospective randomized controlled trial of the safety and feasibility of a novel mesenchymal precursor cell therapy in hypoplastic left heart syndrome, JTCVS Open Volume 16, Dec 2023, doi: https://doi.org/10.1016/j.xjon.2023.09.031 4. Symons JD, Deeter L, Deeter N, et al. Effect of continuous-flow left ventricular assist device support on coronary artery endothelial function in ischemic and nonischemic cardiomyopathy. Cir Heart Fail 2019; 12:e006085. DOI: 10.1161/CIRCHEARTFAILURE.119.006085. 5. Using Reserve Bank of Australia (RBA) published exchange rate from June 30, 2024 of 1A$:0.6624US$. 6. TEMCELL® HS Inj. is a registered trademark of JCR Pharmaceuticals Co. Ltd. 7. TEMCELL sales by our Licensee are recorded in Japanese Yen before being translated into USD for the purposes of calculating the royalty paid to Mesoblast. Results have been adjusted for the movement of the USD to Japanese Yen exchange rate from 1USD:140.01 Yen for the twelve months ended June 30, 2023 to 1USD:151.75 Yen for the twelve months ended June 30, 2024. Forward-Looking Statements This press release includes forward-looking statements that relate to future events or our future financial performance and involve known and unknown risks, uncertainties and other factors that may cause our
簽字人:/s/ Eitan Zamir
名稱:Eitan Zamir

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