Benq Materials Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Benq Materials Corporation has 4 FDA 510(k) cleared medical devices. Based in Taoyuan, TW.
Latest FDA clearance: Apr 2025. Active since 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Benq Materials Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Benq Materials Corporation
4 devices
Cleared
Apr 17, 2025
miacare (DELiGHT daily wear/ DELiGHT 1-day/ CONFiDENCE Color daily...
Ophthalmic
276d
Cleared
May 04, 2020
Anscare SIMO Negative Pressure Wound Therapy (NPWT) System
General & Plastic Surgery
168d
Cleared
Nov 05, 2015
AnsCare ChitoClot Pad
General & Plastic Surgery
209d
Cleared
May 08, 2015
AnsCare ChitoClot Gauze (prescription use), AnsCare ChitoClot Gauze...
General & Plastic Surgery
155d