Endomat Select (UP220)

FDA 510(k) K261706 · Karl Storz Se & Co. KG

Substantially Equivalent

510(k) numberK261706

Submission

Device name
Endomat Select (UP220)
Applicant
Karl Storz Se & Co. KG
Tuttlingen, DE
Received
May 22, 2026
Decision date
July 16, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HIG – Insufflator, Hysteroscopic
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1700
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Endomat Select (UP220) cleared by the FDA?

Endomat Select (UP220) (K261706) received a 510(k) decision of Substantially Equivalent on July 16, 2026, 55 days after the submission was received.

What is the product code of K261706?

The FDA product code is HIG – Insufflator, Hysteroscopic, a Class II (moderate risk) device regulated under 21 CFR 884.1700.