SteriLance Medical (Suzhou), Inc. is one of 1554 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), Heel Incision Safety Lancet (SteriHeel 2), Disposable safety lancet (Impress)
10
Total
10
Cleared
0
Denied
SteriLance Medical (Suzhou), Inc. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Suzhou, CN.
Latest FDA clearance: Jul 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.
FDA 510(k) Regulatory Record - SteriLance Medical (Suzhou), Inc.
10 devices
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