MacroLux Medical Technology Co., Ltd.
MacroLux Medical Technology Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2024, most recent 2026.
Top product codes for MacroLux Medical Technology Co., Ltd.
Recent clearances by MacroLux Medical Technology Co., Ltd.
- K260516 — BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR, C50-CB, C50-CBR)
- K260420 — LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)
- K250452 — CoralWell Single-use Ureteral Access Sheath (NS-0835B, NS-0840B, NS-0845B, NS-0855B, NS-0935B, NS-0940B, NS-0945B, NS-0955B, NS-1035B, NS-1040B, NS-1045B, NS-1055B, NS-1135B, NS-1140B, NS-1145B, NS-1155B, NS-1235B, NS-1240B, NS-1245B, NS-1255B, NS-1335B, NS-1340B, NS-1345B, NS-1355B, NS-1435B, NS-1440B, NS-1445B, NS-1455B)
- K240978 — SeleneView® Single-Use Digital Hysteroscope (HC29, HC29-G, HC35, HC35-G, HO35, HO35-G, HO42, HO42-G)
- K240283 — BubbleView Single-Use Digital Flexible Cystoscope (C50-C, C50-CR, C50-CB, C50-CBR) +1 more
- K233779 — LoopView® Single-Use Digital Flexible Bronchoscope (B38, B38-C, B50, B50-C, B58, B58-C), ViewHub® Video Processor (S13)
- K231774 — CoralView® Single-use Digital Flexible Ureteroscope (6 models)
Data sourced from openFDA. This site is unofficial and independent of the FDA.