SteriLance Medical (Suzhou), Inc. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
SteriLance Medical (Suzhou), Inc. - FDA 510(k) Cleared Devices
Recent clearances: Disposable blood lancet (Soft Pro, Softsure, Softsure Pro, Softsense), Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep), Disposable Blood Lancet (Soft)
11
Total
11
Cleared
0
Denied
SteriLance Medical (Suzhou), Inc. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Suzhou, CN.
Latest FDA clearance: Aug 2026. Active since 2016.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Joyantech Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - SteriLance Medical (Suzhou), Inc.
11 devices
Cleared
Aug 25, 2026
Disposable blood lancet (Soft Pro, Softsure, Softsure Pro, Softsense)
General & Plastic Surgery
27d
Cleared
Jul 06, 2026
Lancing Device (PressGo, LDE3, LDE3AST, LDE5, EasyStep)
General & Plastic Surgery
172d
Cleared
Jun 12, 2026
Disposable Blood Lancet (Soft)
General & Plastic Surgery
25d
Cleared
Feb 26, 2025
Disposable Blood Lancet (Soft Pro)
General & Plastic Surgery
58d
Cleared
Feb 26, 2025
Heel Incision Safety Lancet (SteriHeel 2)
General & Plastic Surgery
58d
Cleared
Jan 16, 2024
Disposable safety lancet (Impress)
General & Plastic Surgery
48d
Cleared
Oct 28, 2022
Disposable Safety Lancet
General & Plastic Surgery
156d
Cleared
Aug 31, 2022
Disposable Blood Lancet
General & Plastic Surgery
100d
Cleared
Aug 30, 2022
Lancing device
General & Plastic Surgery
56d
Cleared
Aug 26, 2021
Heel Incision Safety Lancet
General & Plastic Surgery
167d
Cleared
Aug 29, 2016
Insulin Pen Needle
General Hospital
250d