Medical Device Manufacturer · US , West Boylston , MA

Firstkind Limited - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2014

Total

Cleared

Denied

Firstkind Limited has 11 FDA 510(k) cleared physical medicine devices. Based in West Boylston, US.

Last cleared in 2022. Active since 2014.

Browse the complete list of FDA 510(k) cleared physical medicine devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Firstkind Limited

11 devices

1-11 of 11

Cleared Mar 04, 2022

geko W-3

K220327 · IPF

Physical Medicine · 28d

Cleared Nov 29, 2021

geko W-2

K212762 · IPF

Physical Medicine · 90d

Cleared May 28, 2020

firefly T-2

K201131 · NGX

Physical Medicine · 30d

Cleared Jan 18, 2020

geko™ W-2

K193045 · IPF

Physical Medicine · 78d

Cleared Sep 18, 2019

geko T-2 and geko T-3 Neuromuscular Stimulators

K191113 · IPF

Physical Medicine · 145d

Cleared May 23, 2018

geko T-3 Neuromuscular Stimulator

K181059 · IPF

Physical Medicine · 30d

Cleared Apr 10, 2017

geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators

K163125 · IPF

Physical Medicine · 153d

Cleared Apr 08, 2016

geko(TM) Plus R-2 Neuromuscular Stimulator

K160299 · IPF

Physical Medicine · 64d

Cleared Oct 23, 2015

geko T-2 Neuromuscular Stimulator

K152677 · IPF

Physical Medicine · 35d

Cleared Aug 21, 2014

GEKO

K133638 · IPF

Physical Medicine · 267d

Cleared May 15, 2014

FIREFLY

K134001 · NGX

Physical Medicine · 139d

Firstkind Limited - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Firstkind Limited

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