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 the device name listed in this FDA 510(k) record. The listed applicant is Microsurgical Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-08 under 510(k) 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. The listed applicant is Microsurgical Technologies, Inc.. The 510(k) number is K213173.

When did TrabEx Pro receive FDA 510(k) clearance?

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

Who is the listed applicant for TrabEx Pro?

The FDA 510(k) record lists Microsurgical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TrabEx Pro?

The FDA product code for TrabEx Pro is MRH.

Related Devices (Code: MRH)

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.

K253760OMNI Ultra Surgical System (1-110)Sight Sciences, Inc.K243503VIA360™ Surgical SystemNew World Medical, Inc.K232214OMNI Surgical SystemSight Sciences, Inc.K212797iPrime Viscodelivery SystemGlaukos K211680Streamline Surgical SystemNew World Medical, Inc.K202678OMNI Surgical SystemSight Sciences, Inc.

Official Source

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