ClearanceBrief
Company ยท US

Glooko, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2026. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NBWSystem, Test, Blood Glucose, Over The Counter3
NDCCalculator, Drug Dose2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 1, 2026K260910EndoTool IV Cloud 1.0
Glooko, Inc.
NDC
Feb 2, 2018K171450Glooko Mobile Insulin Dosing System
Glooko, Inc.
NDC
Oct 17, 2013K132272GLOOKO DEVICE SYSTEM FOR GLOOKO APPLICATION
Glooko, Inc.
NBW
Apr 25, 2013K130886GLOOKO DEVICE SYSTEM FOR GLOOKO LOGBOOK+ APPLICATION
Glooko, Inc.
NBW
Dec 21, 2012K122142GLOOKO LOGBOOK CHARTS
Glooko, Inc.
NBW

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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