Stelo Glucose Biosensor System
K-Number: K260935 · 2026-06-12
Device Summary
Frequently Asked Questions
What is the Stelo Glucose Biosensor System?
Stelo Glucose Biosensor System is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Dexcom, Inc.. The 510(k) number is K260935.
When did Stelo Glucose Biosensor System receive FDA 510(k) clearance?
Stelo Glucose Biosensor System received FDA 510(k) clearance on 2026-06-12, under 510(k) number K260935.
Who is the listed applicant for Stelo Glucose Biosensor System?
The FDA 510(k) record lists Dexcom, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stelo Glucose Biosensor System?
The FDA product code for Stelo Glucose Biosensor System is SBH.
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.
Other records listing Dexcom, 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.
Related Devices (Code: SBH)
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.
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.