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FDA PMA

Reherniation reduction device

PMA Number: P160050 · 2026-03-24

ApplicantIntrinsic Therapeutics
Decision Date2026-03-24
PMA NumberP160050
Product CodeQES
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOR

Device Summary

Reherniation reduction device is the device name listed in this FDA 510(k) record. The listed applicant is Intrinsic Therapeutics. It received FDA 510(k) clearance on 2026-03-24. The device is classified under product code QES. It was reviewed by the OR advisory panel.

Frequently Asked Questions

What is the Reherniation reduction device?

Reherniation reduction device is a medical device that received FDA 510(k) clearance on 2026-03-24. The listed applicant is Intrinsic Therapeutics.

When did Reherniation reduction device receive FDA 510(k) clearance?

The clearance date for Reherniation reduction device can be found in the official FDA records.

Who is the listed applicant for Reherniation reduction device?

The FDA 510(k) record lists Intrinsic Therapeutics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reherniation reduction device?

The FDA product code for Reherniation reduction device is QES.

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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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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