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Stryker's Sustainability Solutions
Reprocess in the OR.
- Seven in ten SAGES and EAES surgeons are willing to switch from a first-use to a reprocessed instrument.1
- SSS partners with more than 3,250 facilities acrosss the U.S. and Canada, providing dedicated support to help maintain seamless reprocessing program operations.
- We reprocess over 400 surgical devices from a variety of original device manufacturers (OEM).2
Lower costs. Less waste.
- Support cost savings with Reprocessed LigaSure and Reprocessed HARMONIC scalpels from SSS, while maintaining performance consistent with the original manufacturer's products.3,4
- In 2024, SSS helped customers divert 5 million lbs of waste from landfills.2
- Contact an SSS rep or fill out the form below to learn more about our reprocessing programs.
Featured products
Learn more about the single-use devices that SSS reprocesses.
MyoSure® Hysteroscopy Devices: Sustainable Design
The reprocessed Hologic MyoSure® hysteroscopic tissue...
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References
1. Sathe, Tejas & Alseidi, Nana & Sylla, Patricia. (2024). Perspectives on sustainability among surgeons: findings from the SAGES-EAES sustainability in surgical practice task force survey. Surgical Endoscopy. 38. 5803-5814. 10.1007/s00464-024-11137-7. Proof Comment: Sathe TS, Alseidi A, Bellato V, Ganjouei AA, Foroutani L, Hall RP, Potapov O, Bello RJ, Johnson SM, Marconi S, Francis N, Barach P, Sanchez-Casalongue M, Nijhawan S, Oslock WM, Miller B, Samreen S, Chung J, Marfo N, Huo B, Lim RB, Vandeberg J, Alimi YR, Pietrabissa A, Arezzo A, Frountzas M, Rems M, Eussen MMM, Bouvy ND, Sylla P. Perspectives on sustainability among surgeons: findings from the SAGES-EAES sustainability in surgical practice task force survey. Surg Endosc. 2024 Oct;38(10):5803-5814. doi: 10.1007/s00464-024-11137-7. Epub 2024 Aug 19. PMID: 39160314; PMCID: PMC11458713.
2. Data on file
3. U.S. Food and Drug Administration. 510(k) Premarket Notification: Reprocessed HARMONIC 1100 Shears. K200841. Published May 11, 2020. Accessed February 25, 2025. https://www.accessdata.fda.gov/cdrh_docs/pdf20/K200841.pdf
4. U.S. Food and Drug Administration. 510(k) Premarket Notification: Reprocessed LigaSure Maryland Jaw Sealer/Divider. K180499. Published April 23, 2018. Accessed February 25, 2025.https://www.accessdata.fda.gov/cdrh_docs/pdf18/K180499.pdf https://www.accessdata.fda.gov/cdrh_docs/pdf20/K200841.pdf
SSS-GSNPS-SYK-1679437