ClearanceBrief
Company ยท NZ

Adherium (Nz), Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2023. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CAFNebulizer (Direct Patient Interface)10

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 8, 2023K222247Hailie Sensor NF0110
Adherium (Nz), Ltd., NZ
CAF
Oct 4, 2022K221994Hailie Sensor NF0107 & NF0108
Adherium (Nz), Ltd., NZ
CAF
Jul 15, 2022K220622Hailie Sensor NF0106
Adherium (Nz), Ltd., NZ
CAF
Aug 18, 2021K211233Hailie Sensor NF0109
Adherium (Nz), Ltd., NZ
CAF
Jun 19, 2019K182638Hailie Sensor
Adherium (Nz), Ltd., NZ
CAF
Jun 7, 2019K182573Hailie Sensor
Adherium (Nz), Ltd., NZ
CAF
Dec 10, 2018K181405Hailie Sensor
Adherium (Nz), Ltd., NZ
CAF
Jul 25, 2018K180407Smartinhaler
Adherium (Nz), Ltd., NZ
CAF
Mar 26, 2018K173310SmartTouch
Adherium (Nz), Ltd., NZ
CAF
Aug 30, 2017K163485SmartTouch
Adherium (Nz), Ltd., NZ
CAF

Latest recalls

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