FDA 510(k)

LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)

K-Number: K260420 · 2026-04-08

ApplicantMacroLux Medical Technology Co., Ltd.

Decision Date2026-04-08

Product CodeEOQ

Advisory CommitteeEN

DecisionSubstantially Equivalent

Device Summary

LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG) is the device name listed in this FDA 510(k) record. The listed applicant is MacroLux Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-04-08 under 510(k) number K260420. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)?

LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG) is a medical device that received FDA 510(k) clearance on 2026-04-08. The listed applicant is MacroLux Medical Technology Co., Ltd.. The 510(k) number is K260420.

When did LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG) receive FDA 510(k) clearance?

LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG) received FDA 510(k) clearance on 2026-04-08, under 510(k) number K260420.

Who is the listed applicant for LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)?

The FDA 510(k) record lists MacroLux Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG)?

The FDA product code for LoopView® Single-Use Digital Flexible Bronchoscope (B27-C, B27-CG) is EOQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07630155Office-Based Ureteroscopy Utilizing a Single Use Digital, Flexible Ureteroscope for Upper Tract Urothelial CarcinomaRECRUITING NCT07726784Safety and Feasibility of Medical Thoracoscopy Using Single-use Flexible Bronchoscope Versus SemiRigid Pleuroscope in Pleural EffusionNOT_YET_RECRUITING

Other records listing MacroLux Medical Technology Co., Ltd. as applicant

K260516BubbleView Single-Use Digital Flexible Cystoscope (C38-CS, C38-CRS, C50-C, C50-CR, C50-CB, C50-CBR)K250452CoralWell™ 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)K240978SeleneView® Single-Use Digital Hysteroscope (HC29, HC29-G, HC35, HC35-G, HO35, HO35-G, HO42, HO42-G)K240283BubbleView™ Single-Use Digital Flexible Cystoscope (C50-C, C50-CR, C50-CB, C50-CBR); ViewHub® Video Processor (S13, S13-T, S13-N, S13-S)K233779LoopView® Single-Use Digital Flexible Bronchoscope (B38, B38-C, B50, B50-C, B58, B58-C), ViewHub® Video Processor (S13)K231774CoralView® Single-use Digital Flexible Ureteroscope (U10); CoralView® Single-use Digital Flexible Ureteroscope (U10-B); CoralView® Single-use Digital Flexible Ureteroscope (U10-BR); CoralView® Single-use Digital Flexible Ureteroscope (U20); CoralView® Single-use Digital Flexible Ureteroscope (U20-B); CoralView® Single-use Digital Flexible Ureteroscope (U20-BR)

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Related Devices (Code: EOQ)

K260382MONARCH™ Platform (MON-000008)Auris Health, Inc.K254037LungFlow Airway CatheterFree Flow Medical, Inc.K253137FUJIFILM Endoscope Model EB-840S; FUJIFILM Endoscope Model EB-840TFujifilm Corporation K260565SmartClip Delivery Catheter (ADR-1715)Elucent Medical K252341EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-Q190); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-H190 ); EVIS EXERA III BRONCHOVIDEOSCOPE (OLYMPUS BF-1TH190)Olympus Medical Systems Corp.K250863FUJIFILM Ultrasonic Endoscope EB-710USFujifilm Corporation

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.