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FDA 510(k)

TrabEx Pro

K-Number: K213173 · 2022-06-08

ApplicantMicrosurgical Technologies, Inc.
Decision Date2022-06-08
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TrabEx Pro is a medical device manufactured by Microsurgical Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-08 under approval number K213173. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TrabEx Pro?

TrabEx Pro is a medical device that received FDA 510(k) clearance on 2022-06-08. It is manufactured by Microsurgical Technologies, Inc.. The 510(k) number is K213173.

When was TrabEx Pro approved by the FDA?

TrabEx Pro received FDA 510(k) clearance on 2022-06-08, under approval number K213173.

What company makes TrabEx Pro?

TrabEx Pro is manufactured by Microsurgical Technologies, Inc..

What is the FDA product code for TrabEx Pro?

The FDA product code for TrabEx Pro is MRH.

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K173332OMNI Surgical SystemSight Sciences, Inc. K171905VISCO 360 Viscosurgical SystemSight Sciences, Inc. K201953OMNI PLUS Surgical SystemSight Sciences, Inc. K211680Streamline Surgical SystemNew World Medical, Inc. K202678OMNI Surgical SystemSight Sciences, Inc. K212797iPrime Viscodelivery SystemGlaukos

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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