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.
510(k) submissions have been managed by Jens Medical Consulting, Ltd. as regulatory consultant.
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