510(k) K262581

GraftGun Universal Graft Delivery System (GDS®) by SurGenTec, LLC — Product Code FMF

K262581 is an FDA 510(k) premarket notification submitted by SurGenTec, LLC for the device "GraftGun Universal Graft Delivery System (GDS®)". The FDA issued a decision of Substantially Equivalent on August 26, 2026. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. SurGenTec, LLC has at least 10 other 510(k) clearances on record.