Xiros, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Xiros, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Pitch PaSoft Tissue Reinforcement Device, Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device, Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device
9
Total
9
Cleared
0
Denied
Xiros, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Last cleared in 2023. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Xiros, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Xiros, Ltd.
9 devices
Cleared
May 31, 2023
Pitch PaSoft Tissue Reinforcement Device
General & Plastic Surgery
82d
Cleared
Dec 27, 2022
Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device
Orthopedic
90d
Cleared
Aug 26, 2022
Poly-Tape/Infinity-Lock Soft Tissue Reinforcement Device
General & Plastic Surgery
226d
Cleared
Jul 22, 2022
SECURE-LOCK
Orthopedic
115d
Cleared
Aug 13, 2021
Pitch-Patchs
General & Plastic Surgery
85d
Cleared
Jul 17, 2019
Xtreme-Loop
Orthopedic
89d
Cleared
Apr 03, 2018
Infinity-Lock Button System
Orthopedic
64d
Cleared
Jun 30, 2017
Infinity-Lock 3, Infinity-Lock 5
General & Plastic Surgery
24d
Cleared
Sep 09, 2015
SECURE-LOOP
Orthopedic
89d