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FDA 510(k)

Explant Express

K-Number: K252438 · 2026-02-03

Decision Date2026-02-03
Product CodeQVS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Explant Express is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2026-02-03 under 510(k) number K252438. The device is classified under product code QVS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Explant Express?

Explant Express is a medical device that received FDA 510(k) clearance on 2026-02-03. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K252438.

When did Explant Express receive FDA 510(k) clearance?

Explant Express received FDA 510(k) clearance on 2026-02-03, under 510(k) number K252438.

Who is the listed applicant for Explant Express?

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

What is the FDA product code for Explant Express?

The FDA product code for Explant Express is QVS.

Other records listing Applied Medical Technology, Inc. as applicant

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

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