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FDA 510(k)

TruVision Single-Use 1.9mm Arthroscopy System

K-Number: K260156 · 2026-10-09

ApplicantNexus CMF, LLC
Decision Date2026-10-09
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TruVision Single-Use 1.9mm Arthroscopy System is the device name listed in this FDA 510(k) record. The listed applicant is Nexus CMF, LLC. It received FDA 510(k) clearance on 2026-10-09 under 510(k) number K260156. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TruVision Single-Use 1.9mm Arthroscopy System?

TruVision Single-Use 1.9mm Arthroscopy System is a medical device that received FDA 510(k) clearance on 2026-10-09. The listed applicant is Nexus CMF, LLC. The 510(k) number is K260156.

When did TruVision Single-Use 1.9mm Arthroscopy System receive FDA 510(k) clearance?

TruVision Single-Use 1.9mm Arthroscopy System received FDA 510(k) clearance on 2026-10-09, under 510(k) number K260156.

Who is the listed applicant for TruVision Single-Use 1.9mm Arthroscopy System?

The FDA 510(k) record lists Nexus CMF, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TruVision Single-Use 1.9mm Arthroscopy System?

The FDA product code for TruVision Single-Use 1.9mm Arthroscopy System is HRX.

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.

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Related Devices (Code: HRX)

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.

K260203Fule Vertebroplasty Balloon CatheterBeijing Fule Science & Technology Development Co., Ltd.K254103HOPKINS Telescopes for ArthroscopyKarl Storz SE & CO. KGK252790Digital ClarusScope System and Digital NeuroPEN SystemClarus Medical, LLCK253523Freedom DS™ Decompression SystemSpinal SimplicityK252546VantageTM Lumbar Decompression KitAllevion Medical, LLCK253217MiiS Horus Arthroscope (EJA 100); MiiS Horus Endoscope Display System -Tablet (EDS 500); MiiS Horus Endoscope Display System -Video Box (EVS 700)Medimaging Integrated Solution, Inc (Miis)

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.

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