FDA 510(k) Applications Submitted by Andrea Curria

FDA 510(k) Number	Submission Date	Device Name	Applicant
K191268	05/13/2019	Force Fiber Suture	Teleflex Medical Incorporated
K181774	07/03/2018	Force Fiber White and White/Blue, White/Black, Blue, and White/Green sutures; Force Fiber OrthoTape suture; Bondek suture and Bondek Plus suture; Monodek suture; Polyglytone*6211 suture	Teleflex Medical Incorporated
K233275	09/29/2023	RenaFlex Single-use Flexible Ureteroscope (SUURF-V Standard); RenaFlex Single-use Flexible Ureteroscope (SUURF-VR Reverse); Video System Center for Single-use Endoscopes (CV-S1)	Gyrus ACMI, Inc