ClearanceBrief
Company · GB

Firstkind Limited

FDA 510(k) clearances and medical device recalls filed under this name, 2014 to 2022. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IPFStimulator, Muscle, Powered10
NGXStimulator, Muscle, Powered, For Muscle Conditioning2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 4, 2022K220327geko W-3
Firstkind Limited, GB
IPF
Nov 29, 2021K212762geko W-2
Firstkind Limited, GB
IPF
May 28, 2020K201131firefly T-2
Firstkind Limited, GB
NGX
Jan 18, 2020K193045geko™ W-2
Firstkind Limited, GB
IPF
Sep 18, 2019K191113geko T-2 and geko T-3 Neuromuscular Stimulators
Firstkind Limited, GB
IPF
May 23, 2018K181059geko T-3 Neuromuscular Stimulator
Firstkind Limited, GB
IPF
Feb 11, 2018K180082geko T-2 and geko Plus R-2
Firstkind, Ltd., GB
IPF
Apr 10, 2017K163125geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators
Firstkind Limited, GB
IPF
Apr 8, 2016K160299geko(TM) Plus R-2 Neuromuscular Stimulator
Firstkind Limited, GB
IPF
Oct 23, 2015K152677geko T-2 Neuromuscular Stimulator
Firstkind Limited, GB
IPF
Aug 21, 2014K133638GEKO
Firstkind Limited
IPF
May 15, 2014K134001FIREFLY
Firstkind Limited
NGX

Latest recalls

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