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FDA 510(k)

Everslide

K-Number: K260117 · 2026-09-23

ApplicantSpecial Situations, LLC
Decision Date2026-09-23
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Everslide is the device name listed in this FDA 510(k) record. The listed applicant is Special Situations, LLC. It received FDA 510(k) clearance on 2026-09-23 under 510(k) number K260117. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Everslide?

Everslide is a medical device that received FDA 510(k) clearance on 2026-09-23. The listed applicant is Special Situations, LLC. The 510(k) number is K260117.

When did Everslide receive FDA 510(k) clearance?

Everslide received FDA 510(k) clearance on 2026-09-23, under 510(k) number K260117.

Who is the listed applicant for Everslide?

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

What is the FDA product code for Everslide?

The FDA product code for Everslide is NUC.

Related Devices (Code: NUC)

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

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